Canonical Allele Identifier: CA386888204

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429442G>A (hg19) ; chr12:g.115991637G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991637G>A , CM000674.2:g.115991637G>A	GRCh38
NC_000012.11:g.116429442G>A , CM000674.1:g.116429442G>A	GRCh37
NC_000012.10:g.114913825G>A	NCBI36
NG_023366.1:g.290550C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3317C>T MANE Select	ENSP00000281928.3:p.Ala1106Val
ENST00000549786.2:c.2745C>T
ENST00000648379.1:n.1685C>T
ENST00000648737.1:n.3081C>T
ENST00000648825.1:n.57C>T
ENST00000648916.1:n.1328C>T
ENST00000649607.1:c.1501C>T
ENST00000650226.1:c.3317C>T	ENSP00000496981.1:p.Ala1106Val
ENST00000281928.7:c.3317C>T	ENSP00000281928.3:p.Ala1106Val
NM_015335.4:c.3317C>T	NP_056150.1:p.Ala1106Val
XM_011538080.1:c.3317C>T	XP_011536382.1:p.Ala1106Val
XM_011538081.1:c.3314C>T	XP_011536383.1:p.Ala1105Val
XM_011538082.1:c.3287C>T	XP_011536384.1:p.Ala1096Val
XM_011538080.2:c.3317C>T	XP_011536382.1:p.Ala1106Val
XM_011538081.2:c.3314C>T	XP_011536383.1:p.Ala1105Val
XM_011538082.2:c.3287C>T	XP_011536384.1:p.Ala1096Val
XM_017019090.1:c.3314C>T	XP_016874579.1:p.Ala1105Val
NM_015335.5:c.3317C>T MANE Select	NP_056150.1:p.Ala1106Val