Canonical Allele Identifier: CA6811635

Gene: MED13L

Linked Data

• dbSNP Id: rs761098476
• ExAC: 12:116460292 G / A
• gnomAD v2: 12-116460292-G-A
• MyVariant Identifiers: chr12:g.116460292G>A (hg19) ; chr12:g.116022487G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022487G>A , CM000674.2:g.116022487G>A	GRCh38
NC_000012.11:g.116460292G>A , CM000674.1:g.116460292G>A	GRCh37
NC_000012.10:g.114944675G>A	NCBI36
NG_023366.1:g.259700C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.594C>T MANE Select	ENSP00000281928.3:p.His198=
ENST00000548743.2:c.564C>T	ENSP00000448553.2:p.His188=
ENST00000549786.2:c.22C>T
ENST00000647567.1:c.504C>T	ENSP00000497136.1:p.His168=
ENST00000648737.1:n.358C>T
ENST00000650226.1:c.594C>T	ENSP00000496981.1:p.His198=
ENST00000281928.7:c.594C>T	ENSP00000281928.3:p.His198=
NM_015335.4:c.594C>T	NP_056150.1:p.His198=
XM_011538080.1:c.594C>T	XP_011536382.1:p.His198=
XM_011538081.1:c.594C>T	XP_011536383.1:p.His198=
XM_011538082.1:c.564C>T	XP_011536384.1:p.His188=
XM_011538080.2:c.594C>T	XP_011536382.1:p.His198=
XM_011538081.2:c.594C>T	XP_011536383.1:p.His198=
XM_011538082.2:c.564C>T	XP_011536384.1:p.His188=
XM_017019090.1:c.594C>T	XP_016874579.1:p.His198=
NM_015335.5:c.594C>T MANE Select	NP_056150.1:p.His198=