Canonical Allele Identifier: CA390532463

Gene: NPC2

Linked Data

• ClinVar Variation Id: 1303422
• ClinVar RCV Id: RCV001757977 ; RCV002032783
• dbSNP Id: rs2139668049
• gnomAD v4: 14-74484516-G-A
• MyVariant Identifiers: chr14:g.74951219G>A (hg19) ; chr14:g.74484516G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74484516G>A , CM000676.2:g.74484516G>A	GRCh38
NC_000014.8:g.74951219G>A , CM000676.1:g.74951219G>A	GRCh37
NC_000014.7:g.74020972G>A	NCBI36
NG_007117.1:g.13866C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.262C>T MANE Select	ENSP00000451112.2:p.Pro88Ser
ENST00000238633.6:c.262C>T	ENSP00000238633.2:p.Pro88Ser
ENST00000434013.6:c.262C>T	ENSP00000412103.2:p.Pro88Ser
ENST00000541064.5:c.262C>T	ENSP00000442488.1:p.Pro88Ser
ENST00000553490.5:c.262C>T	ENSP00000451180.1:p.Pro88Ser
ENST00000554482.1:c.158+1813C>T	ENSP00000451314.1:n.158+1813C>T
ENST00000555592.1:c.262C>T	ENSP00000450887.1:p.Pro88Ser
ENST00000555619.5:c.262C>T	ENSP00000451112.1:p.Pro88Ser
ENST00000556009.5:c.327C>T
ENST00000557510.5:c.262C>T	ENSP00000451206.1:p.Pro88Ser
NM_006432.3:c.262C>T	NP_006423.1:p.Pro88Ser
NM_001363688.1:c.262C>T	NP_001350617.1:p.Pro88Ser
NM_006432.4:c.262C>T	NP_006423.1:p.Pro88Ser
NM_001375440.1:c.262C>T	NP_001362369.1:p.Pro88Ser
NM_006432.5:c.262C>T MANE Select	NP_006423.1:p.Pro88Ser