Canonical Allele Identifier: CA2065396664

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997093C= , CM000674.2:g.115997093C=	GRCh38
NC_000012.11:g.116434898C= , CM000674.1:g.116434898C=	GRCh37
NC_000012.10:g.114919281C=	NCBI36
NG_023366.1:g.285094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2707G= MANE Select	ENSP00000281928.3:p.Val903=
ENST00000548743.2:c.2677G=	ENSP00000448553.2:p.Val893=
ENST00000549786.2:c.2135G=
ENST00000647927.1:n.3080G=
ENST00000648173.1:n.1502G=
ENST00000648379.1:n.1075G=
ENST00000648737.1:n.2471G=
ENST00000648916.1:n.718G=
ENST00000649607.1:c.891G=
ENST00000650226.1:c.2707G=	ENSP00000496981.1:p.Val903=
ENST00000281928.7:c.2707G=	ENSP00000281928.3:p.Val903=
NM_015335.4:c.2707G=	NP_056150.1:p.Val903=
XM_011538080.1:c.2707G=	XP_011536382.1:p.Val903=
XM_011538081.1:c.2704G=	XP_011536383.1:p.Val902=
XM_011538082.1:c.2677G=	XP_011536384.1:p.Val893=
XM_011538080.2:c.2707G=	XP_011536382.1:p.Val903=
XM_011538081.2:c.2704G=	XP_011536383.1:p.Val902=
XM_011538082.2:c.2677G=	XP_011536384.1:p.Val893=
XM_017019090.1:c.2704G=	XP_016874579.1:p.Val902=
NM_015335.5:c.2707G= MANE Select	NP_056150.1:p.Val903=