Canonical Allele Identifier: CA2065410888

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970620T= , CM000674.2:g.115970620T=	GRCh38
NC_000012.11:g.116408425T= , CM000674.1:g.116408425T=	GRCh37
NC_000012.10:g.114892808T=	NCBI36
NG_023366.1:g.311567A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6041A= MANE Select	ENSP00000281928.3:p.Asn2014=
ENST00000548784.2:n.2255A=
ENST00000648379.1:n.4409A=
ENST00000648737.1:n.5805A=
ENST00000648825.1:n.4226A=
ENST00000648916.1:n.4052A=
ENST00000649607.1:c.4225A=
ENST00000649775.1:c.2530A=
ENST00000650226.1:c.6077A=	ENSP00000496981.1:p.Asn2026=
ENST00000281928.7:c.6041A=	ENSP00000281928.3:p.Asn2014=
NM_015335.4:c.6041A=	NP_056150.1:p.Asn2014=
XM_011538080.1:c.6077A=	XP_011536382.1:p.Asn2026=
XM_011538081.1:c.6074A=	XP_011536383.1:p.Asn2025=
XM_011538082.1:c.6047A=	XP_011536384.1:p.Asn2016=
XM_011538080.2:c.6077A=	XP_011536382.1:p.Asn2026=
XM_011538081.2:c.6074A=	XP_011536383.1:p.Asn2025=
XM_011538082.2:c.6047A=	XP_011536384.1:p.Asn2016=
XM_017019090.1:c.6038A=	XP_016874579.1:p.Asn2013=
NM_015335.5:c.6041A= MANE Select	NP_056150.1:p.Asn2014=