Canonical Allele Identifier: CA2065381596

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012892T= , CM000674.2:g.116012892T=	GRCh38
NC_000012.11:g.116450697T= , CM000674.1:g.116450697T=	GRCh37
NC_000012.10:g.114935080T=	NCBI36
NG_023366.1:g.269295A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1185A= MANE Select	ENSP00000281928.3:p.Gln395=
ENST00000548743.2:c.1155A=	ENSP00000448553.2:p.Gln385=
ENST00000549786.2:c.613A=
ENST00000647567.1:c.1092A=	ENSP00000497136.1:p.Gln364=
ENST00000648737.1:n.949A=
ENST00000650226.1:c.1185A=	ENSP00000496981.1:p.Gln395=
ENST00000281928.7:c.1185A=	ENSP00000281928.3:p.Gln395=
NM_015335.4:c.1185A=	NP_056150.1:p.Gln395=
XM_011538080.1:c.1185A=	XP_011536382.1:p.Gln395=
XM_011538081.1:c.1185A=	XP_011536383.1:p.Gln395=
XM_011538082.1:c.1155A=	XP_011536384.1:p.Gln385=
XM_011538080.2:c.1185A=	XP_011536382.1:p.Gln395=
XM_011538081.2:c.1185A=	XP_011536383.1:p.Gln395=
XM_011538082.2:c.1155A=	XP_011536384.1:p.Gln385=
XM_017019090.1:c.1185A=	XP_016874579.1:p.Gln395=
NM_015335.5:c.1185A= MANE Select	NP_056150.1:p.Gln395=