Canonical Allele Identifier: CA2584876753
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090808-AGC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090809_4090810del , CM000681.2:g.4090809_4090810del GRCh38
NC_000019.9:g.4090807_4090808del , CM000681.1:g.4090807_4090808del GRCh37
NC_000019.8:g.4041807_4041808del NCBI36
NG_007996.1:g.38319_38320del , LRG_750:g.38319_38320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-102_1532-101del
ENST00000688002.1:n.3244-102_3244-101del
ENST00000688751.1:n.229-102_229-101del
ENST00000689792.1:n.997-102_997-101del
ENST00000262948.10:c.1093-102_1093-101del MANE Select ENSP00000262948.4:n.1093-102_1093-101del
ENST00000262948.9:c.1093-102_1093-101del ENSP00000262948.3:n.1093-102_1093-101del
ENST00000394867.8:c.802-102_802-101del ENSP00000378336.1:n.802-102_802-101del
ENST00000597263.5:n.278-102_278-101del
ENST00000599021.1:c.203-102_203-101del
ENST00000600584.5:n.2542-102_2542-101del
ENST00000601786.5:n.1394-102_1394-101del
NM_030662.3:c.1093-102_1093-101del , LRG_750t1:c.1093-102_1093-101del NP_109587.1:n.1093-102_1093-101del
XM_006722799.2:c.814-102_814-101del XP_006722862.1:n.814-102_814-101del
XM_011528133.1:c.523-102_523-101del XP_011526435.1:n.523-102_523-101del
NM_030662.4:c.1093-102_1093-101del MANE Select NP_109587.1:n.1093-102_1093-101del
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