Canonical Allele Identifier: CA2065386024

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991505G= , CM000674.2:g.115991505G=	GRCh38
NC_000012.11:g.116429310G= , CM000674.1:g.116429310G=	GRCh37
NC_000012.10:g.114913693G=	NCBI36
NG_023366.1:g.290682C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3449C= MANE Select	ENSP00000281928.3:p.Pro1150=
ENST00000549786.2:c.2877C=
ENST00000648379.1:n.1817C=
ENST00000648737.1:n.3213C=
ENST00000648825.1:n.189C=
ENST00000648916.1:n.1460C=
ENST00000649607.1:c.1633C=
ENST00000650226.1:c.3449C=	ENSP00000496981.1:p.Pro1150=
ENST00000281928.7:c.3449C=	ENSP00000281928.3:p.Pro1150=
NM_015335.4:c.3449C=	NP_056150.1:p.Pro1150=
XM_011538080.1:c.3449C=	XP_011536382.1:p.Pro1150=
XM_011538081.1:c.3446C=	XP_011536383.1:p.Pro1149=
XM_011538082.1:c.3419C=	XP_011536384.1:p.Pro1140=
XM_011538080.2:c.3449C=	XP_011536382.1:p.Pro1150=
XM_011538081.2:c.3446C=	XP_011536383.1:p.Pro1149=
XM_011538082.2:c.3419C=	XP_011536384.1:p.Pro1140=
XM_017019090.1:c.3446C=	XP_016874579.1:p.Pro1149=
NM_015335.5:c.3449C= MANE Select	NP_056150.1:p.Pro1150=