Canonical Allele Identifier: CA386927633

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116675467C>A (hg19) ; chr12:g.116237662C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237662C>A , CM000674.2:g.116237662C>A	GRCh38
NC_000012.11:g.116675467C>A , CM000674.1:g.116675467C>A	GRCh37
NC_000012.10:g.115159850C>A	NCBI36
NG_023366.1:g.44525G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.116G>T MANE Select	ENSP00000281928.3:p.Gly39Val
ENST00000548743.2:c.86G>T	ENSP00000448553.2:p.Gly29Val
ENST00000551197.2:c.66G>T
ENST00000647567.1:c.26G>T	ENSP00000497136.1:p.Gly9Val
ENST00000650226.1:c.116G>T	ENSP00000496981.1:p.Gly39Val
ENST00000650375.1:n.278G>T
ENST00000281928.7:c.116G>T	ENSP00000281928.3:p.Gly39Val
ENST00000548743.1:c.86G>T	ENSP00000448553.1:p.Gly29Val
ENST00000551197.1:n.66G>T
NM_015335.4:c.116G>T	NP_056150.1:p.Gly39Val
XM_011538080.1:c.116G>T	XP_011536382.1:p.Gly39Val
XM_011538081.1:c.116G>T	XP_011536383.1:p.Gly39Val
XM_011538082.1:c.86G>T	XP_011536384.1:p.Gly29Val
XM_011538080.2:c.116G>T	XP_011536382.1:p.Gly39Val
XM_011538081.2:c.116G>T	XP_011536383.1:p.Gly39Val
XM_011538082.2:c.86G>T	XP_011536384.1:p.Gly29Val
XM_017019090.1:c.116G>T	XP_016874579.1:p.Gly39Val
NM_015335.5:c.116G>T MANE Select	NP_056150.1:p.Gly39Val