Canonical Allele Identifier: CA2813356111
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090385_4090386insCG , CM000681.2:g.4090385_4090386insCG GRCh38
NC_000019.9:g.4090383_4090384insCG , CM000681.1:g.4090383_4090384insCG GRCh37
NC_000019.8:g.4041383_4041384insCG NCBI36
NG_007996.1:g.38743_38744insCG , LRG_750:g.38743_38744insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1854_1855insCG
ENST00000688751.1:n.551_552insCG
ENST00000689792.1:n.1319_1320insCG
ENST00000262948.10:c.*212_*213insCG MANE Select ENSP00000262948.4:n.*212_*213insCG
ENST00000262948.9:c.*212_*213insCG ENSP00000262948.3:n.*212_*213insCG
ENST00000394867.8:c.*212_*213insCG ENSP00000378336.1:n.*212_*213insCG
ENST00000600584.5:n.2864_2865insCG
ENST00000601786.5:n.1716_1717insCG
NM_030662.3:c.*212_*213insCG , LRG_750t1:c.*212_*213insCG NP_109587.1:n.*212_*213insCG
XM_006722799.2:c.*212_*213insCG XP_006722862.1:n.*212_*213insCG
XM_011528133.1:c.*212_*213insCG XP_011526435.1:n.*212_*213insCG
NM_030662.4:c.*212_*213insCG MANE Select NP_109587.1:n.*212_*213insCG
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