Canonical Allele Identifier: CA390531687
Gene: NPC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74480722A>T , CM000676.2:g.74480722A>T GRCh38
NC_000014.8:g.74947425A>T , CM000676.1:g.74947425A>T GRCh37
NC_000014.7:g.74017178A>T NCBI36
NG_007117.1:g.17660T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555619.6:c.421T>A MANE Select ENSP00000451112.2:p.Trp141Arg
ENST00000238633.6:c.421T>A ENSP00000238633.2:p.Trp141Arg
ENST00000434013.6:c.421T>A ENSP00000412103.2:p.Trp141Arg
ENST00000541064.5:c.364-434T>A ENSP00000442488.1:n.364-434T>A
ENST00000553490.5:c.421T>A ENSP00000451180.1:p.Trp141Arg
ENST00000554482.1:c.216T>A ENSP00000451314.1:n.216T>A
ENST00000555619.5:c.421T>A ENSP00000451112.1:p.Trp141Arg
ENST00000556009.5:c.486T>A
ENST00000557510.5:c.421T>A ENSP00000451206.1:p.Trp141Arg
NM_006432.3:c.421T>A NP_006423.1:p.Trp141Arg
NM_001363688.1:c.421T>A NP_001350617.1:p.Trp141Arg
NM_006432.4:c.421T>A NP_006423.1:p.Trp141Arg
NM_001375440.1:c.364-434T>A NP_001362369.1:n.364-434T>A
NM_006432.5:c.421T>A MANE Select NP_006423.1:p.Trp141Arg