Canonical Allele Identifier: CA2065396735

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997126C= , CM000674.2:g.115997126C=	GRCh38
NC_000012.11:g.116434931C= , CM000674.1:g.116434931C=	GRCh37
NC_000012.10:g.114919314C=	NCBI36
NG_023366.1:g.285061G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2674G= MANE Select	ENSP00000281928.3:p.Val892=
ENST00000548743.2:c.2644G=	ENSP00000448553.2:p.Val882=
ENST00000549786.2:c.2102G=
ENST00000647927.1:n.3047G=
ENST00000648173.1:n.1469G=
ENST00000648379.1:n.1042G=
ENST00000648737.1:n.2438G=
ENST00000648916.1:n.685G=
ENST00000649607.1:c.858G=
ENST00000650226.1:c.2674G=	ENSP00000496981.1:p.Val892=
ENST00000281928.7:c.2674G=	ENSP00000281928.3:p.Val892=
NM_015335.4:c.2674G=	NP_056150.1:p.Val892=
XM_011538080.1:c.2674G=	XP_011536382.1:p.Val892=
XM_011538081.1:c.2671G=	XP_011536383.1:p.Val891=
XM_011538082.1:c.2644G=	XP_011536384.1:p.Val882=
XM_011538080.2:c.2674G=	XP_011536382.1:p.Val892=
XM_011538081.2:c.2671G=	XP_011536383.1:p.Val891=
XM_011538082.2:c.2644G=	XP_011536384.1:p.Val882=
XM_017019090.1:c.2671G=	XP_016874579.1:p.Val891=
NM_015335.5:c.2674G= MANE Select	NP_056150.1:p.Val892=