Canonical Allele Identifier: CA386876679

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408569A>C (hg19) ; chr12:g.115970764A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970764A>C , CM000674.2:g.115970764A>C	GRCh38
NC_000012.11:g.116408569A>C , CM000674.1:g.116408569A>C	GRCh37
NC_000012.10:g.114892952A>C	NCBI36
NG_023366.1:g.311423T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5897T>G MANE Select	ENSP00000281928.3:p.Val1966Gly
ENST00000548694.2:n.887T>G
ENST00000548784.2:n.2111T>G
ENST00000648379.1:n.4265T>G
ENST00000648737.1:n.5661T>G
ENST00000648825.1:n.4082T>G
ENST00000648916.1:n.3908T>G
ENST00000649607.1:c.4081T>G
ENST00000649775.1:c.2386T>G
ENST00000650226.1:c.5933T>G	ENSP00000496981.1:p.Val1978Gly
ENST00000281928.7:c.5897T>G	ENSP00000281928.3:p.Val1966Gly
ENST00000548784.1:n.395T>G
ENST00000552447.1:c.510T>G
NM_015335.4:c.5897T>G	NP_056150.1:p.Val1966Gly
XM_011538080.1:c.5933T>G	XP_011536382.1:p.Val1978Gly
XM_011538081.1:c.5930T>G	XP_011536383.1:p.Val1977Gly
XM_011538082.1:c.5903T>G	XP_011536384.1:p.Val1968Gly
XM_011538080.2:c.5933T>G	XP_011536382.1:p.Val1978Gly
XM_011538081.2:c.5930T>G	XP_011536383.1:p.Val1977Gly
XM_011538082.2:c.5903T>G	XP_011536384.1:p.Val1968Gly
XM_017019090.1:c.5894T>G	XP_016874579.1:p.Val1965Gly
NM_015335.5:c.5897T>G MANE Select	NP_056150.1:p.Val1966Gly