Canonical Allele Identifier: CA8913663
Community Standard Title: NM_000271.5(NPC1):c.695A>G (p.Asp232Gly)
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23560417T>C , CM000680.2:g.23560417T>C GRCh38
NC_000018.9:g.21140381T>C , CM000680.1:g.21140381T>C GRCh37
NC_000018.8:g.19394379T>C NCBI36
NG_012795.1:g.31201A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000271.5:c.695A>G MANE Select NP_000262.2:p.Asp232Gly
ENST00000269228.10:c.695A>G MANE Select ENSP00000269228.4:p.Asp232Gly
NM_000271.4:c.695A>G NP_000262.2:p.Asp232Gly
ENST00000269228.9:c.695A>G ENSP00000269228.4:p.Asp232Gly
ENST00000540608.5:n.609A>G
XM_005258277.1:c.695A>G XP_005258334.1:p.Asp232Gly
XM_005258278.3:c.695A>G XP_005258335.1:p.Asp232Gly
XM_005258278.5:c.695A>G XP_005258335.1:p.Asp232Gly
XM_005258279.1:c.695A>G XP_005258336.1:p.Asp232Gly
XM_005258279.2:c.695A>G XP_005258336.1:p.Asp232Gly
XM_006722479.2:c.695A>G XP_006722542.1:p.Asp232Gly
XM_006722479.3:c.695A>G XP_006722542.1:p.Asp232Gly
XM_011526015.1:c.230A>G XP_011524317.1:p.Asp77Gly
XM_017025784.1:c.695A>G XP_016881273.1:p.Asp232Gly
XM_017025785.1:c.695A>G XP_016881274.1:p.Asp232Gly
XM_017025786.1:c.695A>G XP_016881275.1:p.Asp232Gly
XM_017025787.1:c.695A>G XP_016881276.1:p.Asp232Gly