Canonical Allele Identifier: CA398693959

Gene: MAPK7

Linked Data

• COSMIC: COSM6080403
• MyVariant Identifiers: chr17:g.19286510T>G (hg19) ; chr17:g.19383197T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19383197T>G , CM000679.2:g.19383197T>G	GRCh38
NC_000017.10:g.19286510T>G , CM000679.1:g.19286510T>G	GRCh37
NC_000017.9:g.19227103T>G	NCBI36
NG_027952.1:g.9023A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395604.8:c.2417T>G MANE Select	ENSP00000378968.3:p.Leu806Arg
ENST00000299612.11:c.2000T>G	ENSP00000299612.7:p.Leu667Arg
ENST00000308406.9:c.2417T>G	ENSP00000311005.5:p.Leu806Arg
ENST00000395602.8:c.2417T>G	ENSP00000378966.4:p.Leu806Arg
ENST00000395604.7:c.2417T>G	ENSP00000378968.3:p.Leu806Arg
ENST00000490660.2:n.2520T>G
ENST00000570306.5:n.4192T>G
ENST00000571657.5:n.557T>G
NM_002749.3:c.2417T>G	NP_002740.2:p.Leu806Arg
NM_139032.2:c.2000T>G	NP_620601.1:p.Leu667Arg
NM_139033.2:c.2417T>G	NP_620602.2:p.Leu806Arg
NM_139034.2:c.2417T>G	NP_620603.2:p.Leu806Arg
XM_005256719.2:c.2000T>G	XP_005256776.1:p.Leu667Arg
XM_006721557.2:c.2435T>G	XP_006721620.1:p.Leu812Arg
XM_006721558.2:c.2435T>G	XP_006721621.1:p.Leu812Arg
XM_006721559.2:c.2435T>G	XP_006721622.1:p.Leu812Arg
XM_011523957.1:c.2000T>G	XP_011522259.1:p.Leu667Arg
XM_006721557.3:c.2435T>G	XP_006721620.1:p.Leu812Arg
XM_006721558.3:c.2435T>G	XP_006721621.1:p.Leu812Arg
XM_006721559.3:c.2435T>G	XP_006721622.1:p.Leu812Arg
XM_011523957.3:c.2000T>G	XP_011522259.1:p.Leu667Arg
NM_002749.4:c.2417T>G MANE Select	NP_002740.2:p.Leu806Arg
NM_139032.3:c.2000T>G	NP_620601.1:p.Leu667Arg
NM_139034.3:c.2417T>G	NP_620603.2:p.Leu806Arg
NM_139033.3:c.2417T>G	NP_620602.2:p.Leu806Arg