Canonical Allele Identifier: CA2065504375

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237671T= , CM000674.2:g.116237671T=	GRCh38
NC_000012.11:g.116675476T= , CM000674.1:g.116675476T=	GRCh37
NC_000012.10:g.115159859T=	NCBI36
NG_023366.1:g.44516A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.107A= MANE Select	ENSP00000281928.3:p.Asn36=
ENST00000548743.2:c.77A=	ENSP00000448553.2:p.Asn26=
ENST00000551197.2:c.57A=
ENST00000647567.1:c.17A=	ENSP00000497136.1:p.Asn6=
ENST00000650226.1:c.107A=	ENSP00000496981.1:p.Asn36=
ENST00000650375.1:n.269A=
ENST00000281928.7:c.107A=	ENSP00000281928.3:p.Asn36=
ENST00000548743.1:c.77A=	ENSP00000448553.1:p.Asn26=
ENST00000551197.1:n.57A=
NM_015335.4:c.107A=	NP_056150.1:p.Asn36=
XM_011538080.1:c.107A=	XP_011536382.1:p.Asn36=
XM_011538081.1:c.107A=	XP_011536383.1:p.Asn36=
XM_011538082.1:c.77A=	XP_011536384.1:p.Asn26=
XM_011538080.2:c.107A=	XP_011536382.1:p.Asn36=
XM_011538081.2:c.107A=	XP_011536383.1:p.Asn36=
XM_011538082.2:c.77A=	XP_011536384.1:p.Asn26=
XM_017019090.1:c.107A=	XP_016874579.1:p.Asn36=
NM_015335.5:c.107A= MANE Select	NP_056150.1:p.Asn36=