Canonical Allele Identifier: CA1158990203

Gene: FUCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23865659_23865660delinsTG , CM000663.2:g.23865659_23865660delinsTG	GRCh38
NC_000001.10:g.24192149_24192150delinsTG , CM000663.1:g.24192149_24192150delinsTG	GRCh37
NC_000001.9:g.24064736_24064737delinsTG	NCBI36
NG_013346.1:g.7710_7711delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374479.4:c.390-35_390-34delinsCA MANE Select	ENSP00000363603.3:n.390-35_390-34delinsCA
ENST00000374479.3:c.390-35_390-34delinsCA	ENSP00000363603.3:n.390-35_390-34delinsCA
NM_000147.4:c.390-35_390-34delinsCA	NP_000138.2:n.390-35_390-34delinsCA
XM_005245821.1:c.15-35_15-34delinsCA	XP_005245878.1:n.15-35_15-34delinsCA
XM_011541167.1:c.-244-35_-244-34delinsCA	XP_011539469.1:n.-244-35_-244-34delinsCA
XM_005245821.3:c.15-35_15-34delinsCA	XP_005245878.1:n.15-35_15-34delinsCA
XM_011541167.3:c.-244-35_-244-34delinsCA	XP_011539469.1:n.-244-35_-244-34delinsCA
XM_017000905.2:c.87-35_87-34delinsCA	XP_016856394.1:n.87-35_87-34delinsCA
NM_000147.5:c.390-35_390-34delinsCA MANE Select	NP_000138.2:n.390-35_390-34delinsCA
NR_174379.1:n.568-35_568-34delinsCA
NR_174380.1:n.617-35_617-34delinsCA
NR_174381.1:n.456-35_456-34delinsCA
NR_174382.1:n.853-35_853-34delinsCA