Canonical Allele Identifier: CA398693975

Gene: MAPK7

Linked Data

• MyVariant Identifiers: chr17:g.19286516C>T (hg19) ; chr17:g.19383203C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19383203C>T , CM000679.2:g.19383203C>T	GRCh38
NC_000017.10:g.19286516C>T , CM000679.1:g.19286516C>T	GRCh37
NC_000017.9:g.19227109C>T	NCBI36
NG_027952.1:g.9017G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395604.8:c.2423C>T MANE Select	ENSP00000378968.3:p.Ala808Val
ENST00000299612.11:c.2006C>T	ENSP00000299612.7:p.Ala669Val
ENST00000308406.9:c.2423C>T	ENSP00000311005.5:p.Ala808Val
ENST00000395602.8:c.2423C>T	ENSP00000378966.4:p.Ala808Val
ENST00000395604.7:c.2423C>T	ENSP00000378968.3:p.Ala808Val
ENST00000490660.2:n.2526C>T
ENST00000570306.5:n.4198C>T
ENST00000571657.5:n.563C>T
NM_002749.3:c.2423C>T	NP_002740.2:p.Ala808Val
NM_139032.2:c.2006C>T	NP_620601.1:p.Ala669Val
NM_139033.2:c.2423C>T	NP_620602.2:p.Ala808Val
NM_139034.2:c.2423C>T	NP_620603.2:p.Ala808Val
XM_005256719.2:c.2006C>T	XP_005256776.1:p.Ala669Val
XM_006721557.2:c.2441C>T	XP_006721620.1:p.Ala814Val
XM_006721558.2:c.2441C>T	XP_006721621.1:p.Ala814Val
XM_006721559.2:c.2441C>T	XP_006721622.1:p.Ala814Val
XM_011523957.1:c.2006C>T	XP_011522259.1:p.Ala669Val
XM_006721557.3:c.2441C>T	XP_006721620.1:p.Ala814Val
XM_006721558.3:c.2441C>T	XP_006721621.1:p.Ala814Val
XM_006721559.3:c.2441C>T	XP_006721622.1:p.Ala814Val
XM_011523957.3:c.2006C>T	XP_011522259.1:p.Ala669Val
NM_002749.4:c.2423C>T MANE Select	NP_002740.2:p.Ala808Val
NM_139032.3:c.2006C>T	NP_620601.1:p.Ala669Val
NM_139034.3:c.2423C>T	NP_620603.2:p.Ala808Val
NM_139033.3:c.2423C>T	NP_620602.2:p.Ala808Val