Canonical Allele Identifier: CA2584878000

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095590-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095590C>A , CM000681.2:g.4095590C>A	GRCh38
NC_000019.9:g.4095588C>A , CM000681.1:g.4095588C>A	GRCh37
NC_000019.8:g.4046588C>A	NCBI36
NG_007996.1:g.33539G>T , LRG_750:g.33539G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-141G>T
ENST00000688002.1:n.3136-141G>T
ENST00000688751.1:n.121-141G>T
ENST00000689792.1:n.889-141G>T
ENST00000262948.10:c.985-141G>T MANE Select	ENSP00000262948.4:n.985-141G>T
ENST00000262948.9:c.985-141G>T	ENSP00000262948.3:n.985-141G>T
ENST00000394867.8:c.694-141G>T	ENSP00000378336.1:n.694-141G>T
ENST00000595715.1:n.800-141G>T
ENST00000597263.5:n.170-141G>T
ENST00000599021.1:c.95-141G>T
ENST00000600584.5:n.1545-141G>T
ENST00000601786.5:n.1286-141G>T
NM_030662.3:c.985-141G>T , LRG_750t1:c.985-141G>T	NP_109587.1:n.985-141G>T
XM_006722799.2:c.706-141G>T	XP_006722862.1:n.706-141G>T
XM_011528133.1:c.415-141G>T	XP_011526435.1:n.415-141G>T
XM_017026989.1:c.985-141G>T	XP_016882478.1:n.985-141G>T
XM_017026990.1:c.706-141G>T	XP_016882479.1:n.706-141G>T
NM_030662.4:c.985-141G>T MANE Select	NP_109587.1:n.985-141G>T