Canonical Allele Identifier: CA2584878595

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099516-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099516A>G , CM000681.2:g.4099516A>G	GRCh38
NC_000019.9:g.4099514A>G , CM000681.1:g.4099514A>G	GRCh37
NC_000019.8:g.4050514A>G	NCBI36
NG_007996.1:g.29613T>C , LRG_750:g.29613T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-102T>C
ENST00000687128.1:n.1145-102T>C
ENST00000688002.1:n.898T>C
ENST00000689792.1:n.646-138T>C
ENST00000262948.10:c.706-102T>C MANE Select	ENSP00000262948.4:n.706-102T>C
ENST00000262948.9:c.706-102T>C	ENSP00000262948.3:n.706-102T>C
ENST00000394867.8:c.415-102T>C	ENSP00000378336.1:n.415-102T>C
ENST00000593364.5:n.653-102T>C
ENST00000595715.1:n.419T>C
ENST00000597263.5:n.169+1503T>C
ENST00000599021.1:c.29+1503T>C
ENST00000600584.5:n.1164T>C
ENST00000601786.5:n.1007-102T>C
ENST00000602167.5:n.426-102T>C
NM_030662.3:c.706-102T>C , LRG_750t1:c.706-102T>C	NP_109587.1:n.706-102T>C
XM_006722799.2:c.705+1503T>C	XP_006722862.1:n.705+1503T>C
XM_011528133.1:c.136-102T>C	XP_011526435.1:n.136-102T>C
XM_017026989.1:c.706-102T>C	XP_016882478.1:n.706-102T>C
XM_017026990.1:c.705+1503T>C	XP_016882479.1:n.705+1503T>C
XM_017026991.1:c.*214T>C	XP_016882480.1:n.*214T>C
NM_030662.4:c.706-102T>C MANE Select	NP_109587.1:n.706-102T>C