Canonical Allele Identifier: CA2065396417

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996959A= , CM000674.2:g.115996959A=	GRCh38
NC_000012.11:g.116434764A= , CM000674.1:g.116434764A=	GRCh37
NC_000012.10:g.114919147A=	NCBI36
NG_023366.1:g.285228T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2790+51T= MANE Select	ENSP00000281928.3:n.2790+51T=
ENST00000548743.2:c.2760+51T=	ENSP00000448553.2:n.2760+51T=
ENST00000549786.2:c.2218+51T=
ENST00000647927.1:n.3163+51T=
ENST00000648173.1:n.1585+51T=
ENST00000648379.1:n.1158+51T=
ENST00000648737.1:n.2554+51T=
ENST00000648916.1:n.801+51T=
ENST00000649607.1:c.974+51T=
ENST00000650226.1:c.2790+51T=	ENSP00000496981.1:n.2790+51T=
ENST00000281928.7:c.2790+51T=	ENSP00000281928.3:n.2790+51T=
NM_015335.4:c.2790+51T=	NP_056150.1:n.2790+51T=
XM_011538080.1:c.2790+51T=	XP_011536382.1:n.2790+51T=
XM_011538081.1:c.2787+51T=	XP_011536383.1:n.2787+51T=
XM_011538082.1:c.2760+51T=	XP_011536384.1:n.2760+51T=
XM_011538080.2:c.2790+51T=	XP_011536382.1:n.2790+51T=
XM_011538081.2:c.2787+51T=	XP_011536383.1:n.2787+51T=
XM_011538082.2:c.2760+51T=	XP_011536384.1:n.2760+51T=
XM_017019090.1:c.2787+51T=	XP_016874579.1:n.2787+51T=
NM_015335.5:c.2790+51T= MANE Select	NP_056150.1:n.2790+51T=