Canonical Allele Identifier: CA401785004
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23568865C>A , CM000680.2:g.23568865C>A GRCh38
NC_000018.9:g.21148829C>A , CM000680.1:g.21148829C>A GRCh37
NC_000018.8:g.19402827C>A NCBI36
NG_012795.1:g.22753G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.421G>T MANE Select ENSP00000269228.4:p.Val141Leu
ENST00000269228.9:c.421G>T ENSP00000269228.4:p.Val141Leu
ENST00000540608.5:n.335G>T
NM_000271.4:c.421G>T NP_000262.2:p.Val141Leu
XM_005258277.1:c.421G>T XP_005258334.1:p.Val141Leu
XM_005258278.3:c.421G>T XP_005258335.1:p.Val141Leu
XM_005258279.1:c.421G>T XP_005258336.1:p.Val141Leu
XM_006722479.2:c.421G>T XP_006722542.1:p.Val141Leu
XM_011526015.1:c.-45G>T XP_011524317.1:n.-45G>T
XM_005258278.5:c.421G>T XP_005258335.1:p.Val141Leu
XM_005258279.2:c.421G>T XP_005258336.1:p.Val141Leu
XM_006722479.3:c.421G>T XP_006722542.1:p.Val141Leu
XM_017025784.1:c.421G>T XP_016881273.1:p.Val141Leu
XM_017025785.1:c.421G>T XP_016881274.1:p.Val141Leu
XM_017025786.1:c.421G>T XP_016881275.1:p.Val141Leu
XM_017025787.1:c.421G>T XP_016881276.1:p.Val141Leu
NM_000271.5:c.421G>T MANE Select NP_000262.2:p.Val141Leu