Canonical Allele Identifier: CA390532444

Gene: NPC2

Linked Data

• gnomAD v4: 14-74484507-C-A
• MyVariant Identifiers: chr14:g.74951210C>A (hg19) ; chr14:g.74484507C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74484507C>A , CM000676.2:g.74484507C>A	GRCh38
NC_000014.8:g.74951210C>A , CM000676.1:g.74951210C>A	GRCh37
NC_000014.7:g.74020963C>A	NCBI36
NG_007117.1:g.13875G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.271G>T MANE Select	ENSP00000451112.2:p.Asp91Tyr
ENST00000238633.6:c.271G>T	ENSP00000238633.2:p.Asp91Tyr
ENST00000434013.6:c.271G>T	ENSP00000412103.2:p.Asp91Tyr
ENST00000541064.5:c.271G>T	ENSP00000442488.1:p.Asp91Tyr
ENST00000553490.5:c.271G>T	ENSP00000451180.1:p.Asp91Tyr
ENST00000554482.1:c.158+1822G>T	ENSP00000451314.1:n.158+1822G>T
ENST00000555592.1:c.271G>T	ENSP00000450887.1:p.Asp91Tyr
ENST00000555619.5:c.271G>T	ENSP00000451112.1:p.Asp91Tyr
ENST00000556009.5:c.336G>T
ENST00000557510.5:c.271G>T	ENSP00000451206.1:p.Asp91Tyr
NM_006432.3:c.271G>T	NP_006423.1:p.Asp91Tyr
NM_001363688.1:c.271G>T	NP_001350617.1:p.Asp91Tyr
NM_006432.4:c.271G>T	NP_006423.1:p.Asp91Tyr
NM_001375440.1:c.271G>T	NP_001362369.1:p.Asp91Tyr
NM_006432.5:c.271G>T MANE Select	NP_006423.1:p.Asp91Tyr