Canonical Allele Identifier: CA2636577720

Gene: MAPK7

Linked Data

• gnomAD v4: 17-19383296-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19383296A>C , CM000679.2:g.19383296A>C	GRCh38
NC_000017.10:g.19286609A>C , CM000679.1:g.19286609A>C	GRCh37
NC_000017.9:g.19227202A>C	NCBI36
NG_027952.1:g.8924T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395604.8:c.*65A>C MANE Select	ENSP00000378968.3:n.*65A>C
ENST00000299612.11:c.*65A>C	ENSP00000299612.7:n.*65A>C
ENST00000308406.9:c.*65A>C	ENSP00000311005.5:n.*65A>C
ENST00000395602.8:c.*65A>C	ENSP00000378966.4:n.*65A>C
ENST00000395604.7:c.*65A>C	ENSP00000378968.3:n.*65A>C
ENST00000490660.2:n.2619A>C
ENST00000570306.5:n.4291A>C
ENST00000571657.5:n.656A>C
NM_002749.3:c.*65A>C	NP_002740.2:n.*65A>C
NM_139032.2:c.*65A>C	NP_620601.1:n.*65A>C
NM_139033.2:c.*65A>C	NP_620602.2:n.*65A>C
NM_139034.2:c.*65A>C	NP_620603.2:n.*65A>C
XM_005256719.2:c.*65A>C	XP_005256776.1:n.*65A>C
XM_006721557.2:c.*65A>C	XP_006721620.1:n.*65A>C
XM_006721558.2:c.*65A>C	XP_006721621.1:n.*65A>C
XM_006721559.2:c.*65A>C	XP_006721622.1:n.*65A>C
XM_011523957.1:c.*65A>C	XP_011522259.1:n.*65A>C
XM_006721557.3:c.*65A>C	XP_006721620.1:n.*65A>C
XM_006721558.3:c.*65A>C	XP_006721621.1:n.*65A>C
XM_006721559.3:c.*65A>C	XP_006721622.1:n.*65A>C
XM_011523957.3:c.*65A>C	XP_011522259.1:n.*65A>C
NM_002749.4:c.*65A>C MANE Select	NP_002740.2:n.*65A>C
NM_139032.3:c.*65A>C	NP_620601.1:n.*65A>C
NM_139034.3:c.*65A>C	NP_620603.2:n.*65A>C
NM_139033.3:c.*65A>C	NP_620602.2:n.*65A>C