Canonical Allele Identifier: CA386872304

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116460345C>T (hg19) ; chr12:g.116022540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022540C>T , CM000674.2:g.116022540C>T	GRCh38
NC_000012.11:g.116460345C>T , CM000674.1:g.116460345C>T	GRCh37
NC_000012.10:g.114944728C>T	NCBI36
NG_023366.1:g.259647G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.541G>A MANE Select	ENSP00000281928.3:p.Val181Met
ENST00000548743.2:c.511G>A	ENSP00000448553.2:p.Val171Met
ENST00000647567.1:c.451G>A	ENSP00000497136.1:p.Val151Met
ENST00000648737.1:n.305G>A
ENST00000650226.1:c.541G>A	ENSP00000496981.1:p.Val181Met
ENST00000281928.7:c.541G>A	ENSP00000281928.3:p.Val181Met
NM_015335.4:c.541G>A	NP_056150.1:p.Val181Met
XM_011538080.1:c.541G>A	XP_011536382.1:p.Val181Met
XM_011538081.1:c.541G>A	XP_011536383.1:p.Val181Met
XM_011538082.1:c.511G>A	XP_011536384.1:p.Val171Met
XM_011538080.2:c.541G>A	XP_011536382.1:p.Val181Met
XM_011538081.2:c.541G>A	XP_011536383.1:p.Val181Met
XM_011538082.2:c.511G>A	XP_011536384.1:p.Val171Met
XM_017019090.1:c.541G>A	XP_016874579.1:p.Val181Met
NM_015335.5:c.541G>A MANE Select	NP_056150.1:p.Val181Met