Canonical Allele Identifier: CA2065410882

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970598G= , CM000674.2:g.115970598G=	GRCh38
NC_000012.11:g.116408403G= , CM000674.1:g.116408403G=	GRCh37
NC_000012.10:g.114892786G=	NCBI36
NG_023366.1:g.311589C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6063C= MANE Select	ENSP00000281928.3:p.Asn2021=
ENST00000548784.2:n.2277C=
ENST00000648379.1:n.4431C=
ENST00000648737.1:n.5827C=
ENST00000648825.1:n.4248C=
ENST00000648916.1:n.4074C=
ENST00000649607.1:c.4247C=
ENST00000649775.1:c.2552C=
ENST00000650226.1:c.6099C=	ENSP00000496981.1:p.Asn2033=
ENST00000281928.7:c.6063C=	ENSP00000281928.3:p.Asn2021=
NM_015335.4:c.6063C=	NP_056150.1:p.Asn2021=
XM_011538080.1:c.6099C=	XP_011536382.1:p.Asn2033=
XM_011538081.1:c.6096C=	XP_011536383.1:p.Asn2032=
XM_011538082.1:c.6069C=	XP_011536384.1:p.Asn2023=
XM_011538080.2:c.6099C=	XP_011536382.1:p.Asn2033=
XM_011538081.2:c.6096C=	XP_011536383.1:p.Asn2032=
XM_011538082.2:c.6069C=	XP_011536384.1:p.Asn2023=
XM_017019090.1:c.6060C=	XP_016874579.1:p.Asn2020=
NM_015335.5:c.6063C= MANE Select	NP_056150.1:p.Asn2021=