Canonical Allele Identifier: CA6810604

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975760A>T , CM000674.2:g.115975760A>T	GRCh38
NC_000012.11:g.116413565A>T , CM000674.1:g.116413565A>T	GRCh37
NC_000012.10:g.114897948A>T	NCBI36
NG_023366.1:g.306427T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015335.5:c.5365-22T>A MANE Select	NP_056150.1:n.5365-22T>A
ENST00000281928.9:c.5365-22T>A MANE Select	ENSP00000281928.3:n.5365-22T>A
NM_015335.4:c.5365-22T>A	NP_056150.1:n.5365-22T>A
ENST00000281928.7:c.5365-22T>A	ENSP00000281928.3:n.5365-22T>A
ENST00000548694.1:n.154-22T>A
ENST00000548694.2:n.154-22T>A
ENST00000648379.1:n.3733-22T>A
ENST00000648737.1:n.5129-22T>A
ENST00000648825.1:n.3550-22T>A
ENST00000648916.1:n.3376-22T>A
ENST00000649607.1:c.3549-22T>A
ENST00000649775.1:c.1854-22T>A
ENST00000650226.1:c.5365-22T>A	ENSP00000496981.1:n.5365-22T>A
XM_011538080.1:c.5365-22T>A	XP_011536382.1:n.5365-22T>A
XM_011538080.2:c.5365-22T>A	XP_011536382.1:n.5365-22T>A
XM_011538081.1:c.5362-22T>A	XP_011536383.1:n.5362-22T>A
XM_011538081.2:c.5362-22T>A	XP_011536383.1:n.5362-22T>A
XM_011538082.1:c.5335-22T>A	XP_011536384.1:n.5335-22T>A
XM_011538082.2:c.5335-22T>A	XP_011536384.1:n.5335-22T>A
XM_017019090.1:c.5362-22T>A	XP_016874579.1:n.5362-22T>A