Canonical Allele Identifier: CA390376929

Gene: NPC2

Linked Data

• MyVariant Identifiers: chr14:g.74959959T>C (hg19) ; chr14:g.74493256T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493256T>C , CM000676.2:g.74493256T>C	GRCh38
NC_000014.8:g.74959959T>C , CM000676.1:g.74959959T>C	GRCh37
NC_000014.7:g.74029712T>C	NCBI36
NG_007117.1:g.5126A>G
NG_033074.1:g.4537T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000555619.6:c.19A>G MANE Select	ENSP00000451112.2:p.Thr7Ala
ENST00000238633.6:c.19A>G	ENSP00000238633.2:p.Thr7Ala
ENST00000434013.6:c.19A>G	ENSP00000412103.2:p.Thr7Ala
ENST00000541064.5:c.19A>G	ENSP00000442488.1:p.Thr7Ala
ENST00000553490.5:c.19A>G	ENSP00000451180.1:p.Thr7Ala
ENST00000555592.1:c.19A>G	ENSP00000450887.1:p.Thr7Ala
ENST00000555619.5:c.19A>G	ENSP00000451112.1:p.Thr7Ala
ENST00000556009.5:c.147+775A>G
ENST00000557510.5:c.19A>G	ENSP00000451206.1:p.Thr7Ala
NM_006432.3:c.19A>G	NP_006423.1:p.Thr7Ala
NM_001363688.1:c.19A>G	NP_001350617.1:p.Thr7Ala
NM_006432.4:c.19A>G	NP_006423.1:p.Thr7Ala
NM_001375440.1:c.19A>G	NP_001362369.1:p.Thr7Ala
NM_006432.5:c.19A>G MANE Select	NP_006423.1:p.Thr7Ala