Canonical Allele Identifier: CA398693954

Gene: MAPK7

Linked Data

• MyVariant Identifiers: chr17:g.19286509C>A (hg19) ; chr17:g.19383196C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19383196C>A , CM000679.2:g.19383196C>A	GRCh38
NC_000017.10:g.19286509C>A , CM000679.1:g.19286509C>A	GRCh37
NC_000017.9:g.19227102C>A	NCBI36
NG_027952.1:g.9024G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395604.8:c.2416C>A MANE Select	ENSP00000378968.3:p.Leu806Met
ENST00000299612.11:c.1999C>A	ENSP00000299612.7:p.Leu667Met
ENST00000308406.9:c.2416C>A	ENSP00000311005.5:p.Leu806Met
ENST00000395602.8:c.2416C>A	ENSP00000378966.4:p.Leu806Met
ENST00000395604.7:c.2416C>A	ENSP00000378968.3:p.Leu806Met
ENST00000490660.2:n.2519C>A
ENST00000570306.5:n.4191C>A
ENST00000571657.5:n.556C>A
NM_002749.3:c.2416C>A	NP_002740.2:p.Leu806Met
NM_139032.2:c.1999C>A	NP_620601.1:p.Leu667Met
NM_139033.2:c.2416C>A	NP_620602.2:p.Leu806Met
NM_139034.2:c.2416C>A	NP_620603.2:p.Leu806Met
XM_005256719.2:c.1999C>A	XP_005256776.1:p.Leu667Met
XM_006721557.2:c.2434C>A	XP_006721620.1:p.Leu812Met
XM_006721558.2:c.2434C>A	XP_006721621.1:p.Leu812Met
XM_006721559.2:c.2434C>A	XP_006721622.1:p.Leu812Met
XM_011523957.1:c.1999C>A	XP_011522259.1:p.Leu667Met
XM_006721557.3:c.2434C>A	XP_006721620.1:p.Leu812Met
XM_006721558.3:c.2434C>A	XP_006721621.1:p.Leu812Met
XM_006721559.3:c.2434C>A	XP_006721622.1:p.Leu812Met
XM_011523957.3:c.1999C>A	XP_011522259.1:p.Leu667Met
NM_002749.4:c.2416C>A MANE Select	NP_002740.2:p.Leu806Met
NM_139032.3:c.1999C>A	NP_620601.1:p.Leu667Met
NM_139034.3:c.2416C>A	NP_620603.2:p.Leu806Met
NM_139033.3:c.2416C>A	NP_620602.2:p.Leu806Met