Canonical Allele Identifier: CA2735555270

Gene: ANGPTL6

Linked Data

• dbSNP Id: rs2145178556

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10098458C>G , CM000681.2:g.10098458C>G	GRCh38
NC_000019.9:g.10209134C>G , CM000681.1:g.10209134C>G	GRCh37
NC_000019.8:g.10070134C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000253109.5:c.-10-1885G>C MANE Select	ENSP00000253109.3:n.-10-1885G>C
ENST00000253109.4:c.-10-1885G>C	ENSP00000253109.3:n.-10-1885G>C
ENST00000592641.5:c.-10-1885G>C	ENSP00000467930.1:n.-10-1885G>C
NM_031917.2:c.-10-1885G>C	NP_114123.2:n.-10-1885G>C
XM_005260091.2:c.234-1885G>C	XP_005260148.1:n.234-1885G>C
XM_011528347.1:c.-10-1885G>C	XP_011526649.1:n.-10-1885G>C
XM_011528348.1:c.192-1885G>C	XP_011526650.1:n.192-1885G>C
XM_011528349.1:c.192-1885G>C	XP_011526651.1:n.192-1885G>C
XM_011528350.1:c.-10-1885G>C	XP_011526652.1:n.-10-1885G>C
NM_001321411.1:c.-10-1885G>C	NP_001308340.1:n.-10-1885G>C
XM_005260091.4:c.234-1885G>C	XP_005260148.1:n.234-1885G>C
XM_011528347.3:c.-10-1885G>C	XP_011526649.1:n.-10-1885G>C
XM_011528348.3:c.192-1885G>C	XP_011526650.1:n.192-1885G>C
XM_011528349.3:c.192-1885G>C	XP_011526651.1:n.192-1885G>C
XM_011528350.3:c.-10-1885G>C	XP_011526652.1:n.-10-1885G>C
XM_017027347.2:c.-10-1885G>C	XP_016882836.1:n.-10-1885G>C
XR_002958369.1:n.425-1885G>C
NM_001321411.2:c.-10-1885G>C	NP_001308340.1:n.-10-1885G>C
NM_001387347.1:c.-10-1885G>C	NP_001374276.1:n.-10-1885G>C
NM_001387348.1:c.-10-1885G>C	NP_001374277.1:n.-10-1885G>C
NM_031917.3:c.-10-1885G>C MANE Select	NP_114123.2:n.-10-1885G>C