Canonical Allele Identifier: CA1158990230

Gene: FUCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23865764_23865765delinsAT , CM000663.2:g.23865764_23865765delinsAT	GRCh38
NC_000001.10:g.24192254_24192255delinsAT , CM000663.1:g.24192254_24192255delinsAT	GRCh37
NC_000001.9:g.24064841_24064842delinsAT	NCBI36
NG_013346.1:g.7605_7606delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374479.4:c.390-140_390-139delinsAT MANE Select	ENSP00000363603.3:n.390-140_390-139delinsAT
ENST00000374479.3:c.390-140_390-139delinsAT	ENSP00000363603.3:n.390-140_390-139delinsAT
NM_000147.4:c.390-140_390-139delinsAT	NP_000138.2:n.390-140_390-139delinsAT
XM_005245821.1:c.15-140_15-139delinsAT	XP_005245878.1:n.15-140_15-139delinsAT
XM_011541167.1:c.-244-140_-244-139delinsAT	XP_011539469.1:n.-244-140_-244-139delinsAT
XM_005245821.3:c.15-140_15-139delinsAT	XP_005245878.1:n.15-140_15-139delinsAT
XM_011541167.3:c.-244-140_-244-139delinsAT	XP_011539469.1:n.-244-140_-244-139delinsAT
XM_017000905.2:c.87-140_87-139delinsAT	XP_016856394.1:n.87-140_87-139delinsAT
NM_000147.5:c.390-140_390-139delinsAT MANE Select	NP_000138.2:n.390-140_390-139delinsAT
NR_174379.1:n.568-140_568-139delinsAT
NR_174380.1:n.617-140_617-139delinsAT
NR_174381.1:n.456-140_456-139delinsAT
NR_174382.1:n.853-140_853-139delinsAT