Canonical Allele Identifier: CA416605529
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24192328C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865838C>T , CM000663.2:g.23865838C>T GRCh38
NC_000001.10:g.24192328C>T , CM000663.1:g.24192328C>T GRCh37
NC_000001.9:g.24064915C>T NCBI36
NG_013346.1:g.7532G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.390-213G>A MANE Select ENSP00000363603.3:n.390-213G>A
ENST00000374479.3:c.390-213G>A ENSP00000363603.3:n.390-213G>A
NM_000147.4:c.390-213G>A NP_000138.2:n.390-213G>A
XM_005245821.1:c.15-213G>A XP_005245878.1:n.15-213G>A
XM_011541167.1:c.-245+72G>A XP_011539469.1:n.-245+72G>A
XM_005245821.3:c.15-213G>A XP_005245878.1:n.15-213G>A
XM_011541167.3:c.-245+72G>A XP_011539469.1:n.-245+72G>A
XM_017000905.2:c.87-213G>A XP_016856394.1:n.87-213G>A
NM_000147.5:c.390-213G>A MANE Select NP_000138.2:n.390-213G>A
NR_174379.1:n.568-213G>A
NR_174380.1:n.617-213G>A
NR_174381.1:n.455+72G>A
NR_174382.1:n.852+72G>A