Canonical Allele Identifier: CA487154006

Gene: NPC2

Linked Data

• dbSNP Id: rs150211005
• gnomAD v2: 14-74959957-T-A
• gnomAD v4: 14-74493254-T-A
• MyVariant Identifiers: chr14:g.74959957T>A (hg19) ; chr14:g.74493254T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493254T>A , CM000676.2:g.74493254T>A	GRCh38
NC_000014.8:g.74959957T>A , CM000676.1:g.74959957T>A	GRCh37
NC_000014.7:g.74029710T>A	NCBI36
NG_007117.1:g.5128A>T
NG_033074.1:g.4535T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000555619.6:c.21A>T MANE Select	ENSP00000451112.2:p.Thr7=
ENST00000238633.6:c.21A>T	ENSP00000238633.2:p.Thr7=
ENST00000434013.6:c.21A>T	ENSP00000412103.2:p.Thr7=
ENST00000541064.5:c.21A>T	ENSP00000442488.1:p.Thr7=
ENST00000553490.5:c.21A>T	ENSP00000451180.1:p.Thr7=
ENST00000555592.1:c.21A>T	ENSP00000450887.1:p.Thr7=
ENST00000555619.5:c.21A>T	ENSP00000451112.1:p.Thr7=
ENST00000556009.5:c.147+777A>T
ENST00000557510.5:c.21A>T	ENSP00000451206.1:p.Thr7=
NM_006432.3:c.21A>T	NP_006423.1:p.Thr7=
NM_001363688.1:c.21A>T	NP_001350617.1:p.Thr7=
NM_006432.4:c.21A>T	NP_006423.1:p.Thr7=
NM_001375440.1:c.21A>T	NP_001362369.1:p.Thr7=
NM_006432.5:c.21A>T MANE Select	NP_006423.1:p.Thr7=