Canonical Allele Identifier: CA401792125

Gene: NPC1

Linked Data

• dbSNP Id: rs1598942629
• MyVariant Identifiers: chr18:g.21118530T>G (hg19) ; chr18:g.23538566T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23538566T>G , CM000680.2:g.23538566T>G	GRCh38
NC_000018.9:g.21118530T>G , CM000680.1:g.21118530T>G	GRCh37
NC_000018.8:g.19372528T>G	NCBI36
NG_012795.1:g.53052A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.3017A>C MANE Select	ENSP00000269228.4:p.Asn1006Thr
ENST00000269228.9:c.3017A>C	ENSP00000269228.4:p.Asn1006Thr
ENST00000591051.1:c.2095A>C
ENST00000591075.1:n.650A>C
ENST00000591955.1:n.360A>C
NM_000271.4:c.3017A>C	NP_000262.2:p.Asn1006Thr
XM_005258277.1:c.3068A>C	XP_005258334.1:p.Asn1023Thr
XM_005258278.3:c.3068A>C	XP_005258335.1:p.Asn1023Thr
XM_005258279.1:c.3017A>C	XP_005258336.1:p.Asn1006Thr
XM_006722479.2:c.3068A>C	XP_006722542.1:p.Asn1023Thr
XM_011526015.1:c.2603A>C	XP_011524317.1:p.Asn868Thr
XM_005258278.5:c.3068A>C	XP_005258335.1:p.Asn1023Thr
XM_005258279.2:c.3017A>C	XP_005258336.1:p.Asn1006Thr
XM_006722479.3:c.3068A>C	XP_006722542.1:p.Asn1023Thr
XM_017025784.1:c.3068A>C	XP_016881273.1:p.Asn1023Thr
XM_017025785.1:c.3068A>C	XP_016881274.1:p.Asn1023Thr
XM_017025786.1:c.3017A>C	XP_016881275.1:p.Asn1006Thr
XM_017025787.1:c.3017A>C	XP_016881276.1:p.Asn1006Thr
NM_000271.5:c.3017A>C MANE Select	NP_000262.2:p.Asn1006Thr