Canonical Allele Identifier: CA398693977
Gene: MAPK7 HGNC NCBI

Linked Data

COSMIC: COSM94671

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19383205G>A , CM000679.2:g.19383205G>A GRCh38
NC_000017.10:g.19286518G>A , CM000679.1:g.19286518G>A GRCh37
NC_000017.9:g.19227111G>A NCBI36
NG_027952.1:g.9015C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395604.8:c.2425G>A MANE Select ENSP00000378968.3:p.Asp809Asn
ENST00000299612.11:c.2008G>A ENSP00000299612.7:p.Asp670Asn
ENST00000308406.9:c.2425G>A ENSP00000311005.5:p.Asp809Asn
ENST00000395602.8:c.2425G>A ENSP00000378966.4:p.Asp809Asn
ENST00000395604.7:c.2425G>A ENSP00000378968.3:p.Asp809Asn
ENST00000490660.2:n.2528G>A
ENST00000570306.5:n.4200G>A
ENST00000571657.5:n.565G>A
NM_002749.3:c.2425G>A NP_002740.2:p.Asp809Asn
NM_139032.2:c.2008G>A NP_620601.1:p.Asp670Asn
NM_139033.2:c.2425G>A NP_620602.2:p.Asp809Asn
NM_139034.2:c.2425G>A NP_620603.2:p.Asp809Asn
XM_005256719.2:c.2008G>A XP_005256776.1:p.Asp670Asn
XM_006721557.2:c.2443G>A XP_006721620.1:p.Asp815Asn
XM_006721558.2:c.2443G>A XP_006721621.1:p.Asp815Asn
XM_006721559.2:c.2443G>A XP_006721622.1:p.Asp815Asn
XM_011523957.1:c.2008G>A XP_011522259.1:p.Asp670Asn
XM_006721557.3:c.2443G>A XP_006721620.1:p.Asp815Asn
XM_006721558.3:c.2443G>A XP_006721621.1:p.Asp815Asn
XM_006721559.3:c.2443G>A XP_006721622.1:p.Asp815Asn
XM_011523957.3:c.2008G>A XP_011522259.1:p.Asp670Asn
NM_002749.4:c.2425G>A MANE Select NP_002740.2:p.Asp809Asn
NM_139032.3:c.2008G>A NP_620601.1:p.Asp670Asn
NM_139034.3:c.2425G>A NP_620603.2:p.Asp809Asn
NM_139033.3:c.2425G>A NP_620602.2:p.Asp809Asn