Canonical Allele Identifier: CA631537175
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1161298959
gnomAD v2: 19-4090808-C-CA
gnomAD v3: 19-4090810-C-CA
gnomAD v4: 19-4090810-C-CA
MyVariant Identifiers: chr19:g.4090808_4090809insA (hg19) chr19:g.4090810_4090811insA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090816dup , CM000681.2:g.4090816dup GRCh38
NC_000019.9:g.4090814dup , CM000681.1:g.4090814dup GRCh37
NC_000019.8:g.4041814dup NCBI36
NG_007996.1:g.38318dup , LRG_750:g.38318dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-103dup
ENST00000688002.1:n.3244-103dup
ENST00000688751.1:n.229-103dup
ENST00000689792.1:n.997-103dup
ENST00000262948.10:c.1093-103dup MANE Select ENSP00000262948.4:n.1093-103dup
ENST00000262948.9:c.1093-103dup ENSP00000262948.3:n.1093-103dup
ENST00000394867.8:c.802-103dup ENSP00000378336.1:n.802-103dup
ENST00000597263.5:n.278-103dup
ENST00000599021.1:c.203-103dup
ENST00000600584.5:n.2542-103dup
ENST00000601786.5:n.1394-103dup
NM_030662.3:c.1093-103dup , LRG_750t1:c.1093-103dup NP_109587.1:n.1093-103dup
XM_006722799.2:c.814-103dup XP_006722862.1:n.814-103dup
XM_011528133.1:c.523-103dup XP_011526435.1:n.523-103dup
NM_030662.4:c.1093-103dup MANE Select NP_109587.1:n.1093-103dup
Search 100 bp 5'
Search 100 bp 3'