Canonical Allele Identifier: CA386878754

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116413120T>A (hg19) ; chr12:g.115975315T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975315T>A , CM000674.2:g.115975315T>A	GRCh38
NC_000012.11:g.116413120T>A , CM000674.1:g.116413120T>A	GRCh37
NC_000012.10:g.114897503T>A	NCBI36
NG_023366.1:g.306872A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-2A>T MANE Select	ENSP00000281928.3:n.5589-2A>T
ENST00000548694.2:n.577A>T
ENST00000648379.1:n.3957-2A>T
ENST00000648737.1:n.5353-2A>T
ENST00000648825.1:n.3774-2A>T
ENST00000648916.1:n.3600-2A>T
ENST00000649607.1:c.3773-2A>T
ENST00000649775.1:c.2078-2A>T
ENST00000650226.1:c.5623A>T	ENSP00000496981.1:p.Arg1875Trp
ENST00000281928.7:c.5589-2A>T	ENSP00000281928.3:n.5589-2A>T
ENST00000548694.1:n.577A>T
ENST00000552447.1:c.200A>T
NM_015335.4:c.5589-2A>T	NP_056150.1:n.5589-2A>T
XM_011538080.1:c.5623A>T	XP_011536382.1:p.Arg1875Trp
XM_011538081.1:c.5620A>T	XP_011536383.1:p.Arg1874Trp
XM_011538082.1:c.5593A>T	XP_011536384.1:p.Arg1865Trp
XM_011538080.2:c.5623A>T	XP_011536382.1:p.Arg1875Trp
XM_011538081.2:c.5620A>T	XP_011536383.1:p.Arg1874Trp
XM_011538082.2:c.5593A>T	XP_011536384.1:p.Arg1865Trp
XM_017019090.1:c.5586-2A>T	XP_016874579.1:n.5586-2A>T
NM_015335.5:c.5589-2A>T MANE Select	NP_056150.1:n.5589-2A>T