Canonical Allele Identifier: CA2184679470

Gene: MAP2K5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67794450A= , CM000677.2:g.67794450A=	GRCh38
NC_000015.9:g.68086788A= , CM000677.1:g.68086788A=	GRCh37
NC_000015.8:g.65873842A=	NCBI36
NG_029143.1:g.256768A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000178640.10:c.1243-12196A= MANE Select	ENSP00000178640.5:n.1243-12196A=
ENST00000178640.9:c.1243-12196A=	ENSP00000178640.5:n.1243-12196A=
ENST00000340972.8:c.673-12196A=	ENSP00000342101.4:n.673-12196A=
ENST00000354498.9:c.1135-12196A=	ENSP00000346493.5:n.1135-12196A=
ENST00000395476.6:c.1213-12196A=	ENSP00000378859.2:n.1213-12196A=
ENST00000558274.1:n.327-12196A=
ENST00000558392.5:n.1069-12196A=
NM_001206804.1:c.1135-12196A=	NP_001193733.1:n.1135-12196A=
NM_002757.3:c.1213-12196A=	NP_002748.1:n.1213-12196A=
NM_145160.2:c.1243-12196A=	NP_660143.1:n.1243-12196A=
XM_011521784.1:c.1288-12196A=	XP_011520086.1:n.1288-12196A=
XM_011521786.1:c.1216-12196A=	XP_011520088.1:n.1216-12196A=
XM_024449988.1:c.1012-12196A=	XP_024305756.1:n.1012-12196A=
NM_145160.3:c.1243-12196A= MANE Select	NP_660143.1:n.1243-12196A=
NM_001206804.2:c.1135-12196A=	NP_001193733.1:n.1135-12196A=
NM_002757.4:c.1213-12196A=	NP_002748.1:n.1213-12196A=