Canonical Allele Identifier: CA7268104

Gene: NPC2

Linked Data

• dbSNP Id: rs754836840
• ExAC: 14:74947320 CT / C
• MyVariant Identifiers: chr14:g.74947321del (hg19) ; chr14:g.74480618del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74480619del , CM000676.2:g.74480619del	GRCh38
NC_000014.8:g.74947322del , CM000676.1:g.74947322del	GRCh37
NC_000014.7:g.74017075del	NCBI36
NG_007117.1:g.17764del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.441+84del MANE Select	ENSP00000451112.2:n.441+84del
ENST00000238633.6:c.432+93del	ENSP00000238633.2:n.432+93del
ENST00000434013.6:c.441+84del	ENSP00000412103.2:n.441+84del
ENST00000541064.5:c.364-330del	ENSP00000442488.1:n.364-330del
ENST00000553490.5:c.457+68del	ENSP00000451180.1:n.457+68del
ENST00000554482.1:c.236+84del	ENSP00000451314.1:n.236+84del
ENST00000555619.5:c.441+84del	ENSP00000451112.1:n.441+84del
ENST00000556009.5:c.506+84del
ENST00000557510.5:c.525del	ENSP00000451206.1:p.Ter175=
NM_006432.3:c.441+84del	NP_006423.1:n.441+84del
NM_001363688.1:c.525del	NP_001350617.1:p.Ter175=
NM_006432.4:c.441+84del	NP_006423.1:n.441+84del
NM_001375440.1:c.364-330del	NP_001362369.1:n.364-330del
NM_006432.5:c.441+84del MANE Select	NP_006423.1:n.441+84del