Canonical Allele Identifier: CA403081482
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526852G>C , CM000681.2:g.7526852G>C GRCh38
NC_000019.9:g.7591738G>C , CM000681.1:g.7591738G>C GRCh37
NC_000019.8:g.7497738G>C NCBI36
NG_015806.1:g.9243G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.497G>C MANE Select ENSP00000264079.5:p.Cys166Ser
ENST00000264079.10:c.497G>C ENSP00000264079.5:p.Cys166Ser
ENST00000394321.9:n.577G>C
ENST00000596008.1:n.459G>C
ENST00000598406.1:n.318G>C
ENST00000601003.1:c.497G>C ENSP00000469074.1:p.Cys166Ser
NM_020533.2:c.497G>C NP_065394.1:p.Cys166Ser
NM_020533.3:c.497G>C MANE Select NP_065394.1:p.Cys166Ser