Canonical Allele Identifier: CA2576197358

Gene: MAPK7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19383307C>A , CM000679.2:g.19383307C>A	GRCh38
NC_000017.10:g.19286620C>A , CM000679.1:g.19286620C>A	GRCh37
NC_000017.9:g.19227213C>A	NCBI36
NG_027952.1:g.8913G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395604.8:c.*76C>A MANE Select	ENSP00000378968.3:n.*76C>A
ENST00000299612.11:c.*76C>A	ENSP00000299612.7:n.*76C>A
ENST00000308406.9:c.*76C>A	ENSP00000311005.5:n.*76C>A
ENST00000395602.8:c.*76C>A	ENSP00000378966.4:n.*76C>A
ENST00000395604.7:c.*76C>A	ENSP00000378968.3:n.*76C>A
ENST00000490660.2:n.2630C>A
ENST00000570306.5:n.4302C>A
ENST00000571657.5:n.667C>A
NM_002749.3:c.*76C>A	NP_002740.2:n.*76C>A
NM_139032.2:c.*76C>A	NP_620601.1:n.*76C>A
NM_139033.2:c.*76C>A	NP_620602.2:n.*76C>A
NM_139034.2:c.*76C>A	NP_620603.2:n.*76C>A
XM_005256719.2:c.*76C>A	XP_005256776.1:n.*76C>A
XM_006721557.2:c.*76C>A	XP_006721620.1:n.*76C>A
XM_006721558.2:c.*76C>A	XP_006721621.1:n.*76C>A
XM_006721559.2:c.*76C>A	XP_006721622.1:n.*76C>A
XM_011523957.1:c.*76C>A	XP_011522259.1:n.*76C>A
XM_006721557.3:c.*76C>A	XP_006721620.1:n.*76C>A
XM_006721558.3:c.*76C>A	XP_006721621.1:n.*76C>A
XM_006721559.3:c.*76C>A	XP_006721622.1:n.*76C>A
XM_011523957.3:c.*76C>A	XP_011522259.1:n.*76C>A
NM_002749.4:c.*76C>A MANE Select	NP_002740.2:n.*76C>A
NM_139032.3:c.*76C>A	NP_620601.1:n.*76C>A
NM_139034.3:c.*76C>A	NP_620603.2:n.*76C>A
NM_139033.3:c.*76C>A	NP_620602.2:n.*76C>A