Canonical Allele Identifier: CA386890549

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434888A>T (hg19) ; chr12:g.115997083A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997083A>T , CM000674.2:g.115997083A>T	GRCh38
NC_000012.11:g.116434888A>T , CM000674.1:g.116434888A>T	GRCh37
NC_000012.10:g.114919271A>T	NCBI36
NG_023366.1:g.285104T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2717T>A MANE Select	ENSP00000281928.3:p.Val906Asp
ENST00000548743.2:c.2687T>A	ENSP00000448553.2:p.Val896Asp
ENST00000549786.2:c.2145T>A
ENST00000647927.1:n.3090T>A
ENST00000648173.1:n.1512T>A
ENST00000648379.1:n.1085T>A
ENST00000648737.1:n.2481T>A
ENST00000648916.1:n.728T>A
ENST00000649607.1:c.901T>A
ENST00000650226.1:c.2717T>A	ENSP00000496981.1:p.Val906Asp
ENST00000281928.7:c.2717T>A	ENSP00000281928.3:p.Val906Asp
NM_015335.4:c.2717T>A	NP_056150.1:p.Val906Asp
XM_011538080.1:c.2717T>A	XP_011536382.1:p.Val906Asp
XM_011538081.1:c.2714T>A	XP_011536383.1:p.Val905Asp
XM_011538082.1:c.2687T>A	XP_011536384.1:p.Val896Asp
XM_011538080.2:c.2717T>A	XP_011536382.1:p.Val906Asp
XM_011538081.2:c.2714T>A	XP_011536383.1:p.Val905Asp
XM_011538082.2:c.2687T>A	XP_011536384.1:p.Val896Asp
XM_017019090.1:c.2714T>A	XP_016874579.1:p.Val905Asp
NM_015335.5:c.2717T>A MANE Select	NP_056150.1:p.Val906Asp