Canonical Allele Identifier: CA2585249505

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4117333-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117333G>A , CM000681.2:g.4117333G>A	GRCh38
NC_000019.9:g.4117331G>A , CM000681.1:g.4117331G>A	GRCh37
NC_000019.8:g.4068331G>A	NCBI36
NG_007996.1:g.11796C>T , LRG_750:g.11796C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.742+86C>T
ENST00000687128.1:n.742+86C>T
ENST00000262948.10:c.303+86C>T MANE Select	ENSP00000262948.4:n.303+86C>T
ENST00000262948.9:c.303+86C>T	ENSP00000262948.3:n.303+86C>T
ENST00000394867.8:c.12+86C>T	ENSP00000378336.1:n.12+86C>T
ENST00000599345.1:n.500+86C>T
NM_030662.3:c.303+86C>T , LRG_750t1:c.303+86C>T	NP_109587.1:n.303+86C>T
XM_006722799.2:c.303+86C>T	XP_006722862.1:n.303+86C>T
XM_017026989.1:c.303+86C>T	XP_016882478.1:n.303+86C>T
XM_017026990.1:c.303+86C>T	XP_016882479.1:n.303+86C>T
XM_017026991.1:c.303+86C>T	XP_016882480.1:n.303+86C>T
NM_030662.4:c.303+86C>T MANE Select	NP_109587.1:n.303+86C>T