Canonical Allele Identifier: CA733369869

Gene: FUCA1

Linked Data

• dbSNP Id: rs1464975429
• gnomAD v3: 1-23865901-G-T
• gnomAD v4: 1-23865901-G-T
• MyVariant Identifiers: chr1:g.24192391G>T (hg19) ; chr1:g.23865901G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23865901G>T , CM000663.2:g.23865901G>T	GRCh38
NC_000001.10:g.24192391G>T , CM000663.1:g.24192391G>T	GRCh37
NC_000001.9:g.24064978G>T	NCBI36
NG_013346.1:g.7469C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374479.4:c.390-276C>A MANE Select	ENSP00000363603.3:n.390-276C>A
ENST00000374479.3:c.390-276C>A	ENSP00000363603.3:n.390-276C>A
NM_000147.4:c.390-276C>A	NP_000138.2:n.390-276C>A
XM_005245821.1:c.15-276C>A	XP_005245878.1:n.15-276C>A
XM_011541167.1:c.-245+9C>A	XP_011539469.1:n.-245+9C>A
XM_005245821.3:c.15-276C>A	XP_005245878.1:n.15-276C>A
XM_011541167.3:c.-245+9C>A	XP_011539469.1:n.-245+9C>A
XM_017000905.2:c.87-276C>A	XP_016856394.1:n.87-276C>A
NM_000147.5:c.390-276C>A MANE Select	NP_000138.2:n.390-276C>A
NR_174379.1:n.568-276C>A
NR_174380.1:n.617-276C>A
NR_174381.1:n.455+9C>A
NR_174382.1:n.852+9C>A