Canonical Allele Identifier: CA2621147841

Gene: MED13L

Linked Data

• gnomAD v4: 12-116012793-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012793C>T , CM000674.2:g.116012793C>T	GRCh38
NC_000012.11:g.116450598C>T , CM000674.1:g.116450598C>T	GRCh37
NC_000012.10:g.114934981C>T	NCBI36
NG_023366.1:g.269394G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.1280+4G>A MANE Select	ENSP00000281928.3:n.1280+4G>A
ENST00000548743.2:c.1250+4G>A	ENSP00000448553.2:n.1250+4G>A
ENST00000549786.2:c.708+4G>A
ENST00000647567.1:c.1187+4G>A	ENSP00000497136.1:n.1187+4G>A
ENST00000648737.1:n.1044+4G>A
ENST00000650226.1:c.1280+4G>A	ENSP00000496981.1:n.1280+4G>A
ENST00000281928.7:c.1280+4G>A	ENSP00000281928.3:n.1280+4G>A
NM_015335.4:c.1280+4G>A	NP_056150.1:n.1280+4G>A
XM_011538080.1:c.1280+4G>A	XP_011536382.1:n.1280+4G>A
XM_011538081.1:c.1280+4G>A	XP_011536383.1:n.1280+4G>A
XM_011538082.1:c.1250+4G>A	XP_011536384.1:n.1250+4G>A
XM_011538080.2:c.1280+4G>A	XP_011536382.1:n.1280+4G>A
XM_011538081.2:c.1280+4G>A	XP_011536383.1:n.1280+4G>A
XM_011538082.2:c.1250+4G>A	XP_011536384.1:n.1250+4G>A
XM_017019090.1:c.1280+4G>A	XP_016874579.1:n.1280+4G>A
NM_015335.5:c.1280+4G>A MANE Select	NP_056150.1:n.1280+4G>A