Canonical Allele Identifier: CA416626749
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175147T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848657T>G , CM000663.2:g.23848657T>G GRCh38
NC_000001.10:g.24175147T>G , CM000663.1:g.24175147T>G GRCh37
NC_000001.9:g.24047734T>G NCBI36
NG_013346.1:g.24713A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1152A>C MANE Select ENSP00000363603.3:p.Thr384=
ENST00000374479.3:c.1152A>C ENSP00000363603.3:p.Thr384=
NM_000147.4:c.1152A>C NP_000138.2:p.Thr384=
XM_005245821.1:c.777A>C XP_005245878.1:p.Thr259=
XM_011541167.1:c.519A>C XP_011539469.1:p.Thr173=
XM_005245821.3:c.777A>C XP_005245878.1:p.Thr259=
XM_011541167.3:c.519A>C XP_011539469.1:p.Thr173=
XM_017000905.2:c.849A>C XP_016856394.1:p.Thr283=
NM_000147.5:c.1152A>C MANE Select NP_000138.2:p.Thr384=
NR_174379.1:n.1330A>C
NR_174380.1:n.1379A>C
NR_174381.1:n.1218A>C
NR_174382.1:n.1615A>C