Canonical Allele Identifier: CA416626744
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175141T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848651T>G , CM000663.2:g.23848651T>G GRCh38
NC_000001.10:g.24175141T>G , CM000663.1:g.24175141T>G GRCh37
NC_000001.9:g.24047728T>G NCBI36
NG_013346.1:g.24719A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1158A>C MANE Select ENSP00000363603.3:p.Val386=
ENST00000374479.3:c.1158A>C ENSP00000363603.3:p.Val386=
NM_000147.4:c.1158A>C NP_000138.2:p.Val386=
XM_005245821.1:c.783A>C XP_005245878.1:p.Val261=
XM_011541167.1:c.525A>C XP_011539469.1:p.Val175=
XM_005245821.3:c.783A>C XP_005245878.1:p.Val261=
XM_011541167.3:c.525A>C XP_011539469.1:p.Val175=
XM_017000905.2:c.855A>C XP_016856394.1:p.Val285=
NM_000147.5:c.1158A>C MANE Select NP_000138.2:p.Val386=
NR_174379.1:n.1336A>C
NR_174380.1:n.1385A>C
NR_174381.1:n.1224A>C
NR_174382.1:n.1621A>C