Canonical Allele Identifier: CA129202

Gene: MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131603129C>T , CM000668.2:g.131603129C>T	GRCh38
NC_000006.11:g.131924269C>T , CM000668.1:g.131924269C>T	GRCh37
NC_000006.10:g.131965962C>T	NCBI36
NG_031860.1:g.30095G>A
NG_031860.2:g.30095G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368068.8:c.1832G>A MANE Select	ENSP00000357047.3:p.Arg611Gln
ENST00000354577.8:c.1850G>A	ENSP00000346588.4:p.Arg617Gln
ENST00000368053.8:c.1850G>A	ENSP00000357032.4:p.Arg617Gln
ENST00000368058.5:c.1850G>A	ENSP00000357037.1:p.Arg617Gln
ENST00000368060.7:c.1832G>A	ENSP00000357039.3:p.Arg611Gln
ENST00000368068.7:c.1832G>A	ENSP00000357047.3:p.Arg611Gln
ENST00000539158.1:c.*15G>A	ENSP00000445072.1:n.*15G>A
NM_001270521.1:c.1832G>A	NP_001257450.1:p.Arg611Gln
NM_001270522.1:c.1832G>A	NP_001257451.1:p.Arg611Gln
NM_004830.3:c.1832G>A	NP_004821.2:p.Arg611Gln
NM_015979.3:c.1850G>A	NP_057063.2:p.Arg617Gln
XM_005267223.1:c.1850G>A	XP_005267280.1:p.Arg617Gln
XM_006715612.2:c.1850G>A	XP_006715675.1:p.Arg617Gln
XM_011536257.1:c.1736G>A	XP_011534559.1:p.Arg579Gln
XM_005267223.3:c.1850G>A	XP_005267280.1:p.Arg617Gln
XM_006715612.3:c.1850G>A	XP_006715675.1:p.Arg617Gln
XM_011536257.3:c.1736G>A	XP_011534559.1:p.Arg579Gln
XM_017011501.1:c.899G>A	XP_016866990.1:p.Arg300Gln
NM_004830.4:c.1832G>A MANE Select	NP_004821.2:p.Arg611Gln
NM_001270521.2:c.1832G>A	NP_001257450.1:p.Arg611Gln
NM_001270522.2:c.1832G>A	NP_001257451.1:p.Arg611Gln
NM_001376517.1:c.1850G>A	NP_001363446.1:p.Arg617Gln
NM_001376518.1:c.1778G>A	NP_001363447.1:p.Arg593Gln
NM_001376519.1:c.1832G>A	NP_001363448.1:p.Arg611Gln
NM_001376520.1:c.1691G>A	NP_001363449.1:p.Arg564Gln
NM_001376521.1:c.1832G>A	NP_001363450.1:p.Arg611Gln
NM_001376522.1:c.1832G>A	NP_001363451.1:p.Arg611Gln
NM_001376523.1:c.1577G>A	NP_001363452.1:p.Arg526Gln
NM_001376524.1:c.1832G>A	NP_001363453.1:p.Arg611Gln
NM_015979.4:c.1850G>A	NP_057063.2:p.Arg617Gln