Canonical Allele Identifier: CA2322259970

Gene: ANGPTL6

Linked Data

• dbSNP Id: rs2088597477

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10098416G>T , CM000681.2:g.10098416G>T	GRCh38
NC_000019.9:g.10209092G>T , CM000681.1:g.10209092G>T	GRCh37
NC_000019.8:g.10070092G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000253109.5:c.-10-1843C>A MANE Select	ENSP00000253109.3:n.-10-1843C>A
ENST00000253109.4:c.-10-1843C>A	ENSP00000253109.3:n.-10-1843C>A
ENST00000592641.5:c.-10-1843C>A	ENSP00000467930.1:n.-10-1843C>A
NM_031917.2:c.-10-1843C>A	NP_114123.2:n.-10-1843C>A
XM_005260091.2:c.234-1843C>A	XP_005260148.1:n.234-1843C>A
XM_011528347.1:c.-10-1843C>A	XP_011526649.1:n.-10-1843C>A
XM_011528348.1:c.192-1843C>A	XP_011526650.1:n.192-1843C>A
XM_011528349.1:c.192-1843C>A	XP_011526651.1:n.192-1843C>A
XM_011528350.1:c.-10-1843C>A	XP_011526652.1:n.-10-1843C>A
NM_001321411.1:c.-10-1843C>A	NP_001308340.1:n.-10-1843C>A
XM_005260091.4:c.234-1843C>A	XP_005260148.1:n.234-1843C>A
XM_011528347.3:c.-10-1843C>A	XP_011526649.1:n.-10-1843C>A
XM_011528348.3:c.192-1843C>A	XP_011526650.1:n.192-1843C>A
XM_011528349.3:c.192-1843C>A	XP_011526651.1:n.192-1843C>A
XM_011528350.3:c.-10-1843C>A	XP_011526652.1:n.-10-1843C>A
XM_017027347.2:c.-10-1843C>A	XP_016882836.1:n.-10-1843C>A
XR_002958369.1:n.425-1843C>A
NM_001321411.2:c.-10-1843C>A	NP_001308340.1:n.-10-1843C>A
NM_001387347.1:c.-10-1843C>A	NP_001374276.1:n.-10-1843C>A
NM_001387348.1:c.-10-1843C>A	NP_001374277.1:n.-10-1843C>A
NM_031917.3:c.-10-1843C>A MANE Select	NP_114123.2:n.-10-1843C>A