Canonical Allele Identifier: CA1171146750

Gene: ANGPTL3 DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62597531G= , CM000663.2:g.62597531G=	GRCh38
NC_000001.10:g.63063202G= , CM000663.1:g.63063202G=	GRCh37
NC_000001.9:g.62835790G=	NCBI36
NG_028169.1:g.5016G=
NG_033073.1:g.95838C=
NG_033073.2:g.95838C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371129.4:c.-36G= (ANGPTL3) MANE Select	ENSP00000360170.3:n.-36G=
ENST00000614472.5:c.1389-10907C= (DOCK7)	ENSP00000483062.2:n.1389-10907C=
ENST00000635253.2:c.1683-10907C= (DOCK7) MANE Select	ENSP00000489124.1:n.1683-10907C=
ENST00000637208.1:c.1683-10907C= (DOCK7)	ENSP00000490079.1:n.1683-10907C=
ENST00000637227.1:n.92C= (DOCK7)
ENST00000251157.10:c.1683-10907C= (DOCK7)	ENSP00000251157.6:n.1683-10907C=
ENST00000340370.10:c.1683-10907C= (DOCK7)	ENSP00000340742.5:n.1683-10907C=
ENST00000371129.3:c.-36G= (ANGPTL3)	ENSP00000360170.3:n.-36G=
ENST00000404627.3:c.1683-10907C= (DOCK7)	ENSP00000384446.2:n.1683-10907C=
ENST00000454575.6:c.1683-10907C= (DOCK7)	ENSP00000413583.2:n.1683-10907C=
ENST00000614472.4:c.1359-10907C= (DOCK7)	ENSP00000483062.1:n.1359-10907C=
ENST00000634223.1:c.13-10907C= (DOCK7)
ENST00000634264.1:c.1683-10907C= (DOCK7)	ENSP00000489284.1:n.1683-10907C=
ENST00000635123.1:c.1683-10907C= (DOCK7)	ENSP00000489499.1:n.1683-10907C=
ENST00000635253.1:c.1683-10907C= (DOCK7)	ENSP00000489124.1:n.1683-10907C=
NM_001271999.1:c.1683-10907C= (DOCK7)	NP_001258928.1:n.1683-10907C=
NM_001272000.1:c.1683-10907C= (DOCK7)	NP_001258929.1:n.1683-10907C=
NM_001272001.1:c.1683-10907C= (DOCK7)	NP_001258930.1:n.1683-10907C=
NM_001272002.1:c.1683-10907C= (DOCK7)	NP_001258931.1:n.1683-10907C=
NM_014495.3:c.-36G= (ANGPTL3)	NP_055310.1:n.-36G=
NM_033407.3:c.1683-10907C= (DOCK7)	NP_212132.2:n.1683-10907C=
XM_005271292.1:c.1683-10907C= (DOCK7)	XP_005271349.1:n.1683-10907C=
XM_011542326.1:c.1683-10907C= (DOCK7)	XP_011540628.1:n.1683-10907C=
XM_011542327.1:c.1683-10907C= (DOCK7)	XP_011540629.1:n.1683-10907C=
XM_011542328.1:c.1683-10907C= (DOCK7)	XP_011540630.1:n.1683-10907C=
XM_011542329.1:c.1683-10907C= (DOCK7)	XP_011540631.1:n.1683-10907C=
XM_011542330.1:c.1683-10907C= (DOCK7)	XP_011540632.1:n.1683-10907C=
NM_001330614.1:c.1683-10907C= (DOCK7)	NP_001317543.1:n.1683-10907C=
XM_011542326.2:c.1683-10907C= (DOCK7)	XP_011540628.1:n.1683-10907C=
XM_011542327.2:c.1683-10907C= (DOCK7)	XP_011540629.1:n.1683-10907C=
XM_011542328.2:c.1683-10907C= (DOCK7)	XP_011540630.1:n.1683-10907C=
XM_011542330.2:c.1683-10907C= (DOCK7)	XP_011540632.1:n.1683-10907C=
XM_017002639.1:c.1683-10907C= (DOCK7)	XP_016858128.1:n.1683-10907C=
XM_017002640.1:c.1683-10907C= (DOCK7)	XP_016858129.1:n.1683-10907C=
NM_001367561.1:c.1683-10907C= (DOCK7) MANE Select	NP_001354490.1:n.1683-10907C=
NM_001272002.2:c.1683-10907C= (DOCK7)	NP_001258931.1:n.1683-10907C=
NM_014495.4:c.-36G= (ANGPTL3) MANE Select	NP_055310.1:n.-36G=
NM_001271999.2:c.1683-10907C= (DOCK7)	NP_001258928.1:n.1683-10907C=
NM_001272000.2:c.1683-10907C= (DOCK7)	NP_001258929.1:n.1683-10907C=
NM_001272001.2:c.1683-10907C= (DOCK7)	NP_001258930.1:n.1683-10907C=
NM_001330614.2:c.1683-10907C= (DOCK7)	NP_001317543.1:n.1683-10907C=
NM_033407.4:c.1683-10907C= (DOCK7)	NP_212132.2:n.1683-10907C=