Canonical Allele Identifier: CA386927666

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116675482C>A (hg19) ; chr12:g.116237677C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237677C>A , CM000674.2:g.116237677C>A	GRCh38
NC_000012.11:g.116675482C>A , CM000674.1:g.116675482C>A	GRCh37
NC_000012.10:g.115159865C>A	NCBI36
NG_023366.1:g.44510G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.101G>T MANE Select	ENSP00000281928.3:p.Arg34Met
ENST00000548743.2:c.71G>T	ENSP00000448553.2:p.Arg24Met
ENST00000551197.2:c.51G>T
ENST00000647567.1:c.11G>T	ENSP00000497136.1:p.Arg4Met
ENST00000650226.1:c.101G>T	ENSP00000496981.1:p.Arg34Met
ENST00000650375.1:n.263G>T
ENST00000281928.7:c.101G>T	ENSP00000281928.3:p.Arg34Met
ENST00000548743.1:c.71G>T	ENSP00000448553.1:p.Arg24Met
ENST00000551197.1:n.51G>T
NM_015335.4:c.101G>T	NP_056150.1:p.Arg34Met
XM_011538080.1:c.101G>T	XP_011536382.1:p.Arg34Met
XM_011538081.1:c.101G>T	XP_011536383.1:p.Arg34Met
XM_011538082.1:c.71G>T	XP_011536384.1:p.Arg24Met
XM_011538080.2:c.101G>T	XP_011536382.1:p.Arg34Met
XM_011538081.2:c.101G>T	XP_011536383.1:p.Arg34Met
XM_011538082.2:c.71G>T	XP_011536384.1:p.Arg24Met
XM_017019090.1:c.101G>T	XP_016874579.1:p.Arg34Met
NM_015335.5:c.101G>T MANE Select	NP_056150.1:p.Arg34Met