Canonical Allele Identifier: CA2065385945

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991437C= , CM000674.2:g.115991437C=	GRCh38
NC_000012.11:g.116429242C= , CM000674.1:g.116429242C=	GRCh37
NC_000012.10:g.114913625C=	NCBI36
NG_023366.1:g.290750G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3517G= MANE Select	ENSP00000281928.3:p.Gly1173=
ENST00000549786.2:c.2945G=
ENST00000648379.1:n.1885G=
ENST00000648737.1:n.3281G=
ENST00000648825.1:n.257G=
ENST00000648916.1:n.1528G=
ENST00000649607.1:c.1701G=
ENST00000649775.1:c.14G=
ENST00000650226.1:c.3517G=	ENSP00000496981.1:p.Gly1173=
ENST00000281928.7:c.3517G=	ENSP00000281928.3:p.Gly1173=
NM_015335.4:c.3517G=	NP_056150.1:p.Gly1173=
XM_011538080.1:c.3517G=	XP_011536382.1:p.Gly1173=
XM_011538081.1:c.3514G=	XP_011536383.1:p.Gly1172=
XM_011538082.1:c.3487G=	XP_011536384.1:p.Gly1163=
XM_011538080.2:c.3517G=	XP_011536382.1:p.Gly1173=
XM_011538081.2:c.3514G=	XP_011536383.1:p.Gly1172=
XM_011538082.2:c.3487G=	XP_011536384.1:p.Gly1163=
XM_017019090.1:c.3514G=	XP_016874579.1:p.Gly1172=
NM_015335.5:c.3517G= MANE Select	NP_056150.1:p.Gly1173=