Canonical Allele Identifier: CA2641274006
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23540103_23540104insACC , CM000680.2:g.23540103_23540104insACC GRCh38
NC_000018.9:g.21120067_21120068insACC , CM000680.1:g.21120067_21120068insACC GRCh37
NC_000018.8:g.19374065_19374066insACC NCBI36
NG_012795.1:g.51515_51516insGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2605-102_2605-101insGTG MANE Select ENSP00000269228.4:n.2605-102_2605-101insGTG
ENST00000269228.9:c.2605-102_2605-101insGTG ENSP00000269228.4:n.2605-102_2605-101insGTG
ENST00000540608.5:n.2519-102_2519-101insGTG
ENST00000586718.1:n.396-102_396-101insGTG
ENST00000591051.1:c.1683-102_1683-101insGTG
NM_000271.4:c.2605-102_2605-101insGTG NP_000262.2:n.2605-102_2605-101insGTG
XM_005258277.1:c.2656-102_2656-101insGTG XP_005258334.1:n.2656-102_2656-101insGTG
XM_005258278.3:c.2656-102_2656-101insGTG XP_005258335.1:n.2656-102_2656-101insGTG
XM_005258279.1:c.2605-102_2605-101insGTG XP_005258336.1:n.2605-102_2605-101insGTG
XM_006722479.2:c.2656-102_2656-101insGTG XP_006722542.1:n.2656-102_2656-101insGTG
XM_011526015.1:c.2191-102_2191-101insGTG XP_011524317.1:n.2191-102_2191-101insGTG
XM_005258278.5:c.2656-102_2656-101insGTG XP_005258335.1:n.2656-102_2656-101insGTG
XM_005258279.2:c.2605-102_2605-101insGTG XP_005258336.1:n.2605-102_2605-101insGTG
XM_006722479.3:c.2656-102_2656-101insGTG XP_006722542.1:n.2656-102_2656-101insGTG
XM_017025784.1:c.2656-102_2656-101insGTG XP_016881273.1:n.2656-102_2656-101insGTG
XM_017025785.1:c.2656-102_2656-101insGTG XP_016881274.1:n.2656-102_2656-101insGTG
XM_017025786.1:c.2605-102_2605-101insGTG XP_016881275.1:n.2605-102_2605-101insGTG
XM_017025787.1:c.2605-102_2605-101insGTG XP_016881276.1:n.2605-102_2605-101insGTG
NM_000271.5:c.2605-102_2605-101insGTG MANE Select NP_000262.2:n.2605-102_2605-101insGTG