Canonical Allele Identifier: CA1167984965

Gene: PCSK9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059694_55059695delinsAG , CM000663.2:g.55059694_55059695delinsAG	GRCh38
NC_000001.10:g.55525367_55525368delinsAG , CM000663.1:g.55525367_55525368delinsAG	GRCh37
NC_000001.9:g.55297955_55297956delinsAG	NCBI36
NG_009061.1:g.25148_25149delinsAG , LRG_275:g.25148_25149delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1681+31_1681+32delinsAG	ENSP00000501161.2:n.1681+31_1681+32delinsAG
ENST00000710286.1:c.2038+31_2038+32delinsAG	ENSP00000518176.1:n.2038+31_2038+32delinsAG
ENST00000673903.1:c.1306+31_1306+32delinsAG	ENSP00000501257.1:n.1306+31_1306+32delinsAG
ENST00000673913.1:c.421+31_421+32delinsAG	ENSP00000501161.1:n.421+31_421+32delinsAG
ENST00000302118.5:c.1681+31_1681+32delinsAG MANE Select	ENSP00000303208.5:n.1681+31_1681+32delinsAG
ENST00000490692.1:n.2227+1047_2227+1048delinsAG
NM_174936.3:c.1681+31_1681+32delinsAG , LRG_275t1:c.1681+31_1681+32delinsAG	NP_777596.2:n.1681+31_1681+32delinsAG
NR_110451.1:n.1288+31_1288+32delinsAG
XM_011541193.1:c.802+31_802+32delinsAG	XP_011539495.1:n.802+31_802+32delinsAG
NM_174936.4:c.1681+31_1681+32delinsAG MANE Select	NP_777596.2:n.1681+31_1681+32delinsAG
NR_110451.2:n.1288+31_1288+32delinsAG