Canonical Allele Identifier: CA386876105

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408416C>A (hg19) ; chr12:g.115970611C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970611C>A , CM000674.2:g.115970611C>A	GRCh38
NC_000012.11:g.116408416C>A , CM000674.1:g.116408416C>A	GRCh37
NC_000012.10:g.114892799C>A	NCBI36
NG_023366.1:g.311576G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6050G>T MANE Select	ENSP00000281928.3:p.Gly2017Val
ENST00000548784.2:n.2264G>T
ENST00000648379.1:n.4418G>T
ENST00000648737.1:n.5814G>T
ENST00000648825.1:n.4235G>T
ENST00000648916.1:n.4061G>T
ENST00000649607.1:c.4234G>T
ENST00000649775.1:c.2539G>T
ENST00000650226.1:c.6086G>T	ENSP00000496981.1:p.Gly2029Val
ENST00000281928.7:c.6050G>T	ENSP00000281928.3:p.Gly2017Val
NM_015335.4:c.6050G>T	NP_056150.1:p.Gly2017Val
XM_011538080.1:c.6086G>T	XP_011536382.1:p.Gly2029Val
XM_011538081.1:c.6083G>T	XP_011536383.1:p.Gly2028Val
XM_011538082.1:c.6056G>T	XP_011536384.1:p.Gly2019Val
XM_011538080.2:c.6086G>T	XP_011536382.1:p.Gly2029Val
XM_011538081.2:c.6083G>T	XP_011536383.1:p.Gly2028Val
XM_011538082.2:c.6056G>T	XP_011536384.1:p.Gly2019Val
XM_017019090.1:c.6047G>T	XP_016874579.1:p.Gly2016Val
NM_015335.5:c.6050G>T MANE Select	NP_056150.1:p.Gly2017Val