Canonical Allele Identifier: CA481946570

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420336A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982531A>T , CM000674.2:g.115982531A>T	GRCh38
NC_000012.11:g.116420336A>T , CM000674.1:g.116420336A>T	GRCh37
NC_000012.10:g.114904719A>T	NCBI36
NG_023366.1:g.299656T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5028T>A MANE Select	ENSP00000281928.3:p.Ala1676=
ENST00000549786.2:c.4456T>A
ENST00000648379.1:n.3396T>A
ENST00000648737.1:n.4792T>A
ENST00000648825.1:n.1768T>A
ENST00000648916.1:n.3039T>A
ENST00000649146.1:n.2271T>A
ENST00000649607.1:c.3212T>A
ENST00000649775.1:c.1517T>A
ENST00000650226.1:c.5028T>A	ENSP00000496981.1:p.Ala1676=
ENST00000281928.7:c.5028T>A	ENSP00000281928.3:p.Ala1676=
ENST00000549786.1:c.392T>A
ENST00000552340.1:c.60T>A	ENSP00000449876.1:p.Ala20=
NM_015335.4:c.5028T>A	NP_056150.1:p.Ala1676=
XM_011538080.1:c.5028T>A	XP_011536382.1:p.Ala1676=
XM_011538081.1:c.5025T>A	XP_011536383.1:p.Ala1675=
XM_011538082.1:c.4998T>A	XP_011536384.1:p.Ala1666=
XM_011538080.2:c.5028T>A	XP_011536382.1:p.Ala1676=
XM_011538081.2:c.5025T>A	XP_011536383.1:p.Ala1675=
XM_011538082.2:c.4998T>A	XP_011536384.1:p.Ala1666=
XM_017019090.1:c.5025T>A	XP_016874579.1:p.Ala1675=
NM_015335.5:c.5028T>A MANE Select	NP_056150.1:p.Ala1676=