Canonical Allele Identifier: CA386898280

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116450653G>A (hg19) ; chr12:g.116012848G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012848G>A , CM000674.2:g.116012848G>A	GRCh38
NC_000012.11:g.116450653G>A , CM000674.1:g.116450653G>A	GRCh37
NC_000012.10:g.114935036G>A	NCBI36
NG_023366.1:g.269339C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1229C>T MANE Select	ENSP00000281928.3:p.Ala410Val
ENST00000548743.2:c.1199C>T	ENSP00000448553.2:p.Ala400Val
ENST00000549786.2:c.657C>T
ENST00000647567.1:c.1136C>T	ENSP00000497136.1:p.Ala379Val
ENST00000648737.1:n.993C>T
ENST00000650226.1:c.1229C>T	ENSP00000496981.1:p.Ala410Val
ENST00000281928.7:c.1229C>T	ENSP00000281928.3:p.Ala410Val
NM_015335.4:c.1229C>T	NP_056150.1:p.Ala410Val
XM_011538080.1:c.1229C>T	XP_011536382.1:p.Ala410Val
XM_011538081.1:c.1229C>T	XP_011536383.1:p.Ala410Val
XM_011538082.1:c.1199C>T	XP_011536384.1:p.Ala400Val
XM_011538080.2:c.1229C>T	XP_011536382.1:p.Ala410Val
XM_011538081.2:c.1229C>T	XP_011536383.1:p.Ala410Val
XM_011538082.2:c.1199C>T	XP_011536384.1:p.Ala400Val
XM_017019090.1:c.1229C>T	XP_016874579.1:p.Ala410Val
NM_015335.5:c.1229C>T MANE Select	NP_056150.1:p.Ala410Val