Canonical Allele Identifier: CA8692767

Gene: MED13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61984356A>G , CM000679.2:g.61984356A>G	GRCh38
NC_000017.10:g.60061717A>G , CM000679.1:g.60061717A>G	GRCh37
NC_000017.9:g.57416499A>G	NCBI36
NG_046948.1:g.85956T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397786.7:c.2703T>C MANE Select	ENSP00000380888.2:p.Tyr901=
ENST00000397786.6:c.2703T>C	ENSP00000380888.2:p.Tyr901=
NM_005121.2:c.2703T>C	NP_005112.2:p.Tyr901=
XM_011525551.1:c.2703T>C	XP_011523853.1:p.Tyr901=
XM_011525552.1:c.2703T>C	XP_011523854.1:p.Tyr901=
XM_011525553.1:c.2034T>C	XP_011523855.1:p.Tyr678=
XM_011525554.1:c.372T>C	XP_011523856.1:p.Tyr124=
XM_011525551.2:c.2703T>C	XP_011523853.1:p.Tyr901=
XM_011525552.2:c.2703T>C	XP_011523854.1:p.Tyr901=
XM_011525553.3:c.2034T>C	XP_011523855.1:p.Tyr678=
NM_005121.3:c.2703T>C MANE Select	NP_005112.2:p.Tyr901=