Canonical Allele Identifier: CA2573150176

Gene: NPC2

Linked Data

• ClinVar Variation Id: 1559673
• ClinVar RCV Id: RCV002208952
• dbSNP Id: rs372464598

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74480693T>A , CM000676.2:g.74480693T>A	GRCh38
NC_000014.8:g.74947396T>A , CM000676.1:g.74947396T>A	GRCh37
NC_000014.7:g.74017149T>A	NCBI36
NG_007117.1:g.17689A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.441+9A>T MANE Select	ENSP00000451112.2:n.441+9A>T
ENST00000238633.6:c.432+18A>T	ENSP00000238633.2:n.432+18A>T
ENST00000434013.6:c.441+9A>T	ENSP00000412103.2:n.441+9A>T
ENST00000541064.5:c.364-405A>T	ENSP00000442488.1:n.364-405A>T
ENST00000553490.5:c.450A>T	ENSP00000451180.1:p.Leu150=
ENST00000554482.1:c.236+9A>T	ENSP00000451314.1:n.236+9A>T
ENST00000555619.5:c.441+9A>T	ENSP00000451112.1:n.441+9A>T
ENST00000556009.5:c.506+9A>T
ENST00000557510.5:c.450A>T	ENSP00000451206.1:p.Leu150=
NM_006432.3:c.441+9A>T	NP_006423.1:n.441+9A>T
NM_001363688.1:c.450A>T	NP_001350617.1:p.Leu150=
NM_006432.4:c.441+9A>T	NP_006423.1:n.441+9A>T
NM_001375440.1:c.364-405A>T	NP_001362369.1:n.364-405A>T
NM_006432.5:c.441+9A>T MANE Select	NP_006423.1:n.441+9A>T