Canonical Allele Identifier: CA416691267
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24194678A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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