Canonical Allele Identifier: CA2065396539

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997022G= , CM000674.2:g.115997022G=	GRCh38
NC_000012.11:g.116434827G= , CM000674.1:g.116434827G=	GRCh37
NC_000012.10:g.114919210G=	NCBI36
NG_023366.1:g.285165C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2778C= MANE Select	ENSP00000281928.3:p.Pro926=
ENST00000548743.2:c.2748C=	ENSP00000448553.2:p.Pro916=
ENST00000549786.2:c.2206C=
ENST00000647927.1:n.3151C=
ENST00000648173.1:n.1573C=
ENST00000648379.1:n.1146C=
ENST00000648737.1:n.2542C=
ENST00000648916.1:n.789C=
ENST00000649607.1:c.962C=
ENST00000650226.1:c.2778C=	ENSP00000496981.1:p.Pro926=
ENST00000281928.7:c.2778C=	ENSP00000281928.3:p.Pro926=
NM_015335.4:c.2778C=	NP_056150.1:p.Pro926=
XM_011538080.1:c.2778C=	XP_011536382.1:p.Pro926=
XM_011538081.1:c.2775C=	XP_011536383.1:p.Pro925=
XM_011538082.1:c.2748C=	XP_011536384.1:p.Pro916=
XM_011538080.2:c.2778C=	XP_011536382.1:p.Pro926=
XM_011538081.2:c.2775C=	XP_011536383.1:p.Pro925=
XM_011538082.2:c.2748C=	XP_011536384.1:p.Pro916=
XM_017019090.1:c.2775C=	XP_016874579.1:p.Pro925=
NM_015335.5:c.2778C= MANE Select	NP_056150.1:p.Pro926=