Canonical Allele Identifier: CA2584876572

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090503-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090503_4090504insA , CM000681.2:g.4090503_4090504insA	GRCh38
NC_000019.9:g.4090501_4090502insA , CM000681.1:g.4090501_4090502insA	GRCh37
NC_000019.8:g.4041501_4041502insA	NCBI36
NG_007996.1:g.38625_38626insT , LRG_750:g.38625_38626insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1736_1737insT
ENST00000688002.1:n.3448_3449insT
ENST00000688751.1:n.433_434insT
ENST00000689792.1:n.1201_1202insT
ENST00000262948.10:c.*94_*95insT MANE Select	ENSP00000262948.4:n.*94_*95insT
ENST00000262948.9:c.*94_*95insT	ENSP00000262948.3:n.*94_*95insT
ENST00000394867.8:c.*94_*95insT	ENSP00000378336.1:n.*94_*95insT
ENST00000597263.5:n.482_483insT
ENST00000600584.5:n.2746_2747insT
ENST00000601786.5:n.1598_1599insT
NM_030662.3:c.*94_*95insT , LRG_750t1:c.*94_*95insT	NP_109587.1:n.*94_*95insT
XM_006722799.2:c.*94_*95insT	XP_006722862.1:n.*94_*95insT
XM_011528133.1:c.*94_*95insT	XP_011526435.1:n.*94_*95insT
NM_030662.4:c.*94_*95insT MANE Select	NP_109587.1:n.*94_*95insT