Canonical Allele Identifier: CA2065395992

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996742G= , CM000674.2:g.115996742G=	GRCh38
NC_000012.11:g.116434547G= , CM000674.1:g.116434547G=	GRCh37
NC_000012.10:g.114918930G=	NCBI36
NG_023366.1:g.285445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2791-61C= MANE Select	ENSP00000281928.3:n.2791-61C=
ENST00000548743.2:c.2761-61C=	ENSP00000448553.2:n.2761-61C=
ENST00000549786.2:c.2219-61C=
ENST00000647927.1:n.3164-61C=
ENST00000648173.1:n.1586-61C=
ENST00000648379.1:n.1159-61C=
ENST00000648737.1:n.2555-61C=
ENST00000648916.1:n.802-61C=
ENST00000649607.1:c.975-61C=
ENST00000650226.1:c.2791-61C=	ENSP00000496981.1:n.2791-61C=
ENST00000281928.7:c.2791-61C=	ENSP00000281928.3:n.2791-61C=
NM_015335.4:c.2791-61C=	NP_056150.1:n.2791-61C=
XM_011538080.1:c.2791-61C=	XP_011536382.1:n.2791-61C=
XM_011538081.1:c.2788-61C=	XP_011536383.1:n.2788-61C=
XM_011538082.1:c.2761-61C=	XP_011536384.1:n.2761-61C=
XM_011538080.2:c.2791-61C=	XP_011536382.1:n.2791-61C=
XM_011538081.2:c.2788-61C=	XP_011536383.1:n.2788-61C=
XM_011538082.2:c.2761-61C=	XP_011536384.1:n.2761-61C=
XM_017019090.1:c.2788-61C=	XP_016874579.1:n.2788-61C=
NM_015335.5:c.2791-61C= MANE Select	NP_056150.1:n.2791-61C=