Canonical Allele Identifier: CA7268193
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74486433G>C , CM000676.2:g.74486433G>C GRCh38
NC_000014.8:g.74953136G>C , CM000676.1:g.74953136G>C GRCh37
NC_000014.7:g.74022889G>C NCBI36
NG_007117.1:g.11949C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555619.6:c.86C>G MANE Select ENSP00000451112.2:p.Ser29Cys
ENST00000238633.6:c.86C>G ENSP00000238633.2:p.Ser29Cys
ENST00000434013.6:c.86C>G ENSP00000412103.2:p.Ser29Cys
ENST00000541064.5:c.86C>G ENSP00000442488.1:p.Ser29Cys
ENST00000553490.5:c.86C>G ENSP00000451180.1:p.Ser29Cys
ENST00000554482.1:c.54C>G ENSP00000451314.1:p.Phe18Leu
ENST00000555592.1:c.86C>G ENSP00000450887.1:p.Ser29Cys
ENST00000555619.5:c.86C>G ENSP00000451112.1:p.Ser29Cys
ENST00000556009.5:c.151C>G
ENST00000557510.5:c.86C>G ENSP00000451206.1:p.Ser29Cys
NM_006432.3:c.86C>G NP_006423.1:p.Ser29Cys
NM_001363688.1:c.86C>G NP_001350617.1:p.Ser29Cys
NM_006432.4:c.86C>G NP_006423.1:p.Ser29Cys
NM_001375440.1:c.86C>G NP_001362369.1:p.Ser29Cys
NM_006432.5:c.86C>G MANE Select NP_006423.1:p.Ser29Cys