Canonical Allele Identifier: CA999597383
Gene: FUCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1639614080
gnomAD v3: 1-23865906-G-A
gnomAD v4: 1-23865906-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865906G>A , CM000663.2:g.23865906G>A GRCh38
NC_000001.10:g.24192396G>A , CM000663.1:g.24192396G>A GRCh37
NC_000001.9:g.24064983G>A NCBI36
NG_013346.1:g.7464C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.390-281C>T MANE Select ENSP00000363603.3:n.390-281C>T
ENST00000374479.3:c.390-281C>T ENSP00000363603.3:n.390-281C>T
NM_000147.4:c.390-281C>T NP_000138.2:n.390-281C>T
XM_005245821.1:c.15-281C>T XP_005245878.1:n.15-281C>T
XM_011541167.1:c.-245+4C>T XP_011539469.1:n.-245+4C>T
XM_005245821.3:c.15-281C>T XP_005245878.1:n.15-281C>T
XM_011541167.3:c.-245+4C>T XP_011539469.1:n.-245+4C>T
XM_017000905.2:c.87-281C>T XP_016856394.1:n.87-281C>T
NM_000147.5:c.390-281C>T MANE Select NP_000138.2:n.390-281C>T
NR_174379.1:n.568-281C>T
NR_174380.1:n.617-281C>T
NR_174381.1:n.455+4C>T
NR_174382.1:n.852+4C>T