Canonical Allele Identifier: CA339010598
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24194682T>G (hg19) chr1:g.23868192T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23868192T>G , CM000663.2:g.23868192T>G GRCh38
NC_000001.10:g.24194682T>G , CM000663.1:g.24194682T>G GRCh37
NC_000001.9:g.24067269T>G NCBI36
NG_013346.1:g.5178A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.95A>C MANE Select ENSP00000363603.3:p.Gln32Pro
ENST00000374479.3:c.95A>C ENSP00000363603.3:p.Gln32Pro
NM_000147.4:c.95A>C NP_000138.2:p.Gln32Pro
XM_005245821.1:c.-455A>C XP_005245878.1:n.-455A>C
XM_005245821.3:c.-455A>C XP_005245878.1:n.-455A>C
NM_000147.5:c.95A>C MANE Select NP_000138.2:p.Gln32Pro
NR_174379.1:n.99A>C
NR_174380.1:n.99A>C
NR_174381.1:n.99A>C
NR_174382.1:n.99A>C
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