Canonical Allele Identifier: CA2584877813

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095287-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095287A>T , CM000681.2:g.4095287A>T	GRCh38
NC_000019.9:g.4095285A>T , CM000681.1:g.4095285A>T	GRCh37
NC_000019.8:g.4046285A>T	NCBI36
NG_007996.1:g.33842T>A , LRG_750:g.33842T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+101T>A
ENST00000688002.1:n.3197+101T>A
ENST00000688751.1:n.182+101T>A
ENST00000689792.1:n.950+101T>A
ENST00000262948.10:c.1046+101T>A MANE Select	ENSP00000262948.4:n.1046+101T>A
ENST00000262948.9:c.1046+101T>A	ENSP00000262948.3:n.1046+101T>A
ENST00000394867.8:c.755+101T>A	ENSP00000378336.1:n.755+101T>A
ENST00000597263.5:n.231+101T>A
ENST00000599021.1:c.156+101T>A
ENST00000600584.5:n.1707T>A
ENST00000601786.5:n.1347+101T>A
NM_030662.3:c.1046+101T>A , LRG_750t1:c.1046+101T>A	NP_109587.1:n.1046+101T>A
XM_006722799.2:c.767+101T>A	XP_006722862.1:n.767+101T>A
XM_011528133.1:c.476+101T>A	XP_011526435.1:n.476+101T>A
XM_017026989.1:c.1046+101T>A	XP_016882478.1:n.1046+101T>A
XM_017026990.1:c.767+101T>A	XP_016882479.1:n.767+101T>A
NM_030662.4:c.1046+101T>A MANE Select	NP_109587.1:n.1046+101T>A