Canonical Allele Identifier: CA2065386992

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991885C= , CM000674.2:g.115991885C=	GRCh38
NC_000012.11:g.116429690C= , CM000674.1:g.116429690C=	GRCh37
NC_000012.10:g.114914073C=	NCBI36
NG_023366.1:g.290302G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3069G= MANE Select	ENSP00000281928.3:p.Thr1023=
ENST00000548743.2:c.3039G=	ENSP00000448553.2:p.Thr1013=
ENST00000549786.2:c.2497G=
ENST00000648173.1:n.1864G=
ENST00000648379.1:n.1437G=
ENST00000648737.1:n.2833G=
ENST00000648916.1:n.1080G=
ENST00000649607.1:c.1253G=
ENST00000650226.1:c.3069G=	ENSP00000496981.1:p.Thr1023=
ENST00000281928.7:c.3069G=	ENSP00000281928.3:p.Thr1023=
NM_015335.4:c.3069G=	NP_056150.1:p.Thr1023=
XM_011538080.1:c.3069G=	XP_011536382.1:p.Thr1023=
XM_011538081.1:c.3066G=	XP_011536383.1:p.Thr1022=
XM_011538082.1:c.3039G=	XP_011536384.1:p.Thr1013=
XM_011538080.2:c.3069G=	XP_011536382.1:p.Thr1023=
XM_011538081.2:c.3066G=	XP_011536383.1:p.Thr1022=
XM_011538082.2:c.3039G=	XP_011536384.1:p.Thr1013=
XM_017019090.1:c.3066G=	XP_016874579.1:p.Thr1022=
NM_015335.5:c.3069G= MANE Select	NP_056150.1:p.Thr1023=