Canonical Allele Identifier: CA2584878297

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099134-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099134C>T , CM000681.2:g.4099134C>T	GRCh38
NC_000019.9:g.4099132C>T , CM000681.1:g.4099132C>T	GRCh37
NC_000019.8:g.4050132C>T	NCBI36
NG_007996.1:g.29995G>A , LRG_750:g.29995G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1358+67G>A
ENST00000687128.1:n.1425G>A
ENST00000688002.1:n.1280G>A
ENST00000689792.1:n.823+67G>A
ENST00000262948.10:c.919+67G>A MANE Select	ENSP00000262948.4:n.919+67G>A
ENST00000262948.9:c.919+67G>A	ENSP00000262948.3:n.919+67G>A
ENST00000394867.8:c.628+67G>A	ENSP00000378336.1:n.628+67G>A
ENST00000595715.1:n.734+67G>A
ENST00000597263.5:n.169+1885G>A
ENST00000599021.1:c.30-1791G>A
ENST00000600584.5:n.1479+67G>A
ENST00000601786.5:n.1220+67G>A
NM_030662.3:c.919+67G>A , LRG_750t1:c.919+67G>A	NP_109587.1:n.919+67G>A
XM_006722799.2:c.705+1885G>A	XP_006722862.1:n.705+1885G>A
XM_011528133.1:c.349+67G>A	XP_011526435.1:n.349+67G>A
XM_017026989.1:c.919+67G>A	XP_016882478.1:n.919+67G>A
XM_017026990.1:c.705+1885G>A	XP_016882479.1:n.705+1885G>A
NM_030662.4:c.919+67G>A MANE Select	NP_109587.1:n.919+67G>A