Canonical Allele Identifier: CA416691266
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24194678A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23868188A>T , CM000663.2:g.23868188A>T GRCh38
NC_000001.10:g.24194678A>T , CM000663.1:g.24194678A>T GRCh37
NC_000001.9:g.24067265A>T NCBI36
NG_013346.1:g.5182T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.99T>A MANE Select ENSP00000363603.3:p.Pro33=
ENST00000374479.3:c.99T>A ENSP00000363603.3:p.Pro33=
NM_000147.4:c.99T>A NP_000138.2:p.Pro33=
XM_005245821.1:c.-451T>A XP_005245878.1:n.-451T>A
XM_005245821.3:c.-451T>A XP_005245878.1:n.-451T>A
NM_000147.5:c.99T>A MANE Select NP_000138.2:p.Pro33=
NR_174379.1:n.103T>A
NR_174380.1:n.103T>A
NR_174381.1:n.103T>A
NR_174382.1:n.103T>A