Canonical Allele Identifier: CA629591390

Gene: MEX3C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51192166G>T , CM000680.2:g.51192166G>T	GRCh38
NC_000018.9:g.48718536G>T , CM000680.1:g.48718536G>T	GRCh37
NC_000018.8:g.46972534G>T	NCBI36
NG_015801.1:g.10516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406189.4:c.754+4401C>A MANE Select	ENSP00000385610.3:n.754+4401C>A
ENST00000591040.2:c.-107-14590C>A	ENSP00000502049.1:n.-107-14590C>A
ENST00000406189.3:c.754+4401C>A	ENSP00000385610.3:n.754+4401C>A
ENST00000591040.1:n.44-14590C>A
ENST00000616921.1:c.244+4401C>A	ENSP00000482566.1:n.244+4401C>A
NM_016626.4:c.754+4401C>A	NP_057710.3:n.754+4401C>A
NM_016626.5:c.754+4401C>A MANE Select	NP_057710.3:n.754+4401C>A