Canonical Allele Identifier: CA785228210

Gene: MCUB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109669323G>A , CM000666.2:g.109669323G>A	GRCh38
NC_000004.11:g.110590479G>A , CM000666.1:g.110590479G>A	GRCh37
NC_000004.10:g.110809928G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394650.7:c.451+4929G>A MANE Select	ENSP00000378145.4:n.451+4929G>A
ENST00000394650.6:c.451+4929G>A	ENSP00000378145.4:n.451+4929G>A
ENST00000452915.3:n.546+4929G>A
ENST00000472310.5:n.580+4929G>A
NM_017918.4:c.451+4929G>A	NP_060388.2:n.451+4929G>A
XM_006714246.2:c.364+4929G>A	XP_006714309.1:n.364+4929G>A
XM_006714246.3:c.364+4929G>A	XP_006714309.1:n.364+4929G>A
NM_017918.5:c.451+4929G>A MANE Select	NP_060388.2:n.451+4929G>A