Canonical Allele Identifier: CA8440866

Gene: MAPK7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19382063C>T , CM000679.2:g.19382063C>T	GRCh38
NC_000017.10:g.19285376C>T , CM000679.1:g.19285376C>T	GRCh37
NC_000017.9:g.19225969C>T	NCBI36
NG_027952.1:g.10157G>A
NG_031885.1:g.1120G>A
NG_031885.2:g.1131G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002749.4:c.1760C>T MANE Select	NP_002740.2:p.Pro587Leu
ENST00000395604.8:c.1760C>T MANE Select	ENSP00000378968.3:p.Pro587Leu
NM_002749.3:c.1760C>T	NP_002740.2:p.Pro587Leu
NM_139032.2:c.1343C>T	NP_620601.1:p.Pro448Leu
NM_139032.3:c.1343C>T	NP_620601.1:p.Pro448Leu
NM_139033.2:c.1760C>T	NP_620602.2:p.Pro587Leu
NM_139033.3:c.1760C>T	NP_620602.2:p.Pro587Leu
NM_139034.2:c.1760C>T	NP_620603.2:p.Pro587Leu
NM_139034.3:c.1760C>T	NP_620603.2:p.Pro587Leu
ENST00000299612.11:c.1343C>T	ENSP00000299612.7:p.Pro448Leu
ENST00000308406.9:c.1760C>T	ENSP00000311005.5:p.Pro587Leu
ENST00000395602.8:c.1760C>T	ENSP00000378966.4:p.Pro587Leu
ENST00000395604.7:c.1760C>T	ENSP00000378968.3:p.Pro587Leu
ENST00000490660.2:n.1863C>T
ENST00000570306.5:n.3535C>T
ENST00000571657.5:n.304-750C>T
ENST00000573417.1:n.393C>T
XM_005256719.2:c.1343C>T	XP_005256776.1:p.Pro448Leu
XM_006721557.2:c.1778C>T	XP_006721620.1:p.Pro593Leu
XM_006721557.3:c.1778C>T	XP_006721620.1:p.Pro593Leu
XM_006721558.2:c.1778C>T	XP_006721621.1:p.Pro593Leu
XM_006721558.3:c.1778C>T	XP_006721621.1:p.Pro593Leu
XM_006721559.2:c.1778C>T	XP_006721622.1:p.Pro593Leu
XM_006721559.3:c.1778C>T	XP_006721622.1:p.Pro593Leu
XM_011523957.1:c.1343C>T	XP_011522259.1:p.Pro448Leu
XM_011523957.3:c.1343C>T	XP_011522259.1:p.Pro448Leu