Canonical Allele Identifier: CA386898218

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116450624T>C (hg19) ; chr12:g.116012819T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012819T>C , CM000674.2:g.116012819T>C	GRCh38
NC_000012.11:g.116450624T>C , CM000674.1:g.116450624T>C	GRCh37
NC_000012.10:g.114935007T>C	NCBI36
NG_023366.1:g.269368A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1258A>G MANE Select	ENSP00000281928.3:p.Arg420Gly
ENST00000548743.2:c.1228A>G	ENSP00000448553.2:p.Arg410Gly
ENST00000549786.2:c.686A>G
ENST00000647567.1:c.1165A>G	ENSP00000497136.1:p.Arg389Gly
ENST00000648737.1:n.1022A>G
ENST00000650226.1:c.1258A>G	ENSP00000496981.1:p.Arg420Gly
ENST00000281928.7:c.1258A>G	ENSP00000281928.3:p.Arg420Gly
NM_015335.4:c.1258A>G	NP_056150.1:p.Arg420Gly
XM_011538080.1:c.1258A>G	XP_011536382.1:p.Arg420Gly
XM_011538081.1:c.1258A>G	XP_011536383.1:p.Arg420Gly
XM_011538082.1:c.1228A>G	XP_011536384.1:p.Arg410Gly
XM_011538080.2:c.1258A>G	XP_011536382.1:p.Arg420Gly
XM_011538081.2:c.1258A>G	XP_011536383.1:p.Arg420Gly
XM_011538082.2:c.1228A>G	XP_011536384.1:p.Arg410Gly
XM_017019090.1:c.1258A>G	XP_016874579.1:p.Arg420Gly
NM_015335.5:c.1258A>G MANE Select	NP_056150.1:p.Arg420Gly