Canonical Allele Identifier: CA386898196

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116450615A>T (hg19) ; chr12:g.116012810A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012810A>T , CM000674.2:g.116012810A>T	GRCh38
NC_000012.11:g.116450615A>T , CM000674.1:g.116450615A>T	GRCh37
NC_000012.10:g.114934998A>T	NCBI36
NG_023366.1:g.269377T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1267T>A MANE Select	ENSP00000281928.3:p.Cys423Ser
ENST00000548743.2:c.1237T>A	ENSP00000448553.2:p.Cys413Ser
ENST00000549786.2:c.695T>A
ENST00000647567.1:c.1174T>A	ENSP00000497136.1:p.Cys392Ser
ENST00000648737.1:n.1031T>A
ENST00000650226.1:c.1267T>A	ENSP00000496981.1:p.Cys423Ser
ENST00000281928.7:c.1267T>A	ENSP00000281928.3:p.Cys423Ser
NM_015335.4:c.1267T>A	NP_056150.1:p.Cys423Ser
XM_011538080.1:c.1267T>A	XP_011536382.1:p.Cys423Ser
XM_011538081.1:c.1267T>A	XP_011536383.1:p.Cys423Ser
XM_011538082.1:c.1237T>A	XP_011536384.1:p.Cys413Ser
XM_011538080.2:c.1267T>A	XP_011536382.1:p.Cys423Ser
XM_011538081.2:c.1267T>A	XP_011536383.1:p.Cys423Ser
XM_011538082.2:c.1237T>A	XP_011536384.1:p.Cys413Ser
XM_017019090.1:c.1267T>A	XP_016874579.1:p.Cys423Ser
NM_015335.5:c.1267T>A MANE Select	NP_056150.1:p.Cys423Ser