Canonical Allele Identifier: CA2290179860

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23568833_23568835delinsACT , CM000680.2:g.23568833_23568835delinsACT	GRCh38
NC_000018.9:g.21148797_21148799delinsACT , CM000680.1:g.21148797_21148799delinsACT	GRCh37
NC_000018.8:g.19402795_19402797delinsACT	NCBI36
NG_012795.1:g.22783_22785delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.451_453delinsAGT MANE Select	ENSP00000269228.4:p.Ser151=
ENST00000269228.9:c.451_453delinsAGT	ENSP00000269228.4:p.Ser151=
ENST00000540608.5:n.365_367delinsAGT
NM_000271.4:c.451_453delinsAGT	NP_000262.2:p.Ser151=
XM_005258277.1:c.451_453delinsAGT	XP_005258334.1:p.Ser151=
XM_005258278.3:c.451_453delinsAGT	XP_005258335.1:p.Ser151=
XM_005258279.1:c.451_453delinsAGT	XP_005258336.1:p.Ser151=
XM_006722479.2:c.451_453delinsAGT	XP_006722542.1:p.Ser151=
XM_011526015.1:c.-15_-13delinsAGT	XP_011524317.1:n.-15_-13delinsAGT
XM_005258278.5:c.451_453delinsAGT	XP_005258335.1:p.Ser151=
XM_005258279.2:c.451_453delinsAGT	XP_005258336.1:p.Ser151=
XM_006722479.3:c.451_453delinsAGT	XP_006722542.1:p.Ser151=
XM_017025784.1:c.451_453delinsAGT	XP_016881273.1:p.Ser151=
XM_017025785.1:c.451_453delinsAGT	XP_016881274.1:p.Ser151=
XM_017025786.1:c.451_453delinsAGT	XP_016881275.1:p.Ser151=
XM_017025787.1:c.451_453delinsAGT	XP_016881276.1:p.Ser151=
NM_000271.5:c.451_453delinsAGT MANE Select	NP_000262.2:p.Ser151=