Canonical Allele Identifier: CA403152364
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524981C>T , CM000681.2:g.7524981C>T GRCh38
NC_000019.9:g.7589867C>T , CM000681.1:g.7589867C>T GRCh37
NC_000019.8:g.7495867C>T NCBI36
NG_015806.1:g.7372C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.52C>T MANE Select ENSP00000264079.5:p.Pro18Ser
ENST00000264079.10:c.52C>T ENSP00000264079.5:p.Pro18Ser
ENST00000394321.9:n.132C>T
ENST00000596390.1:n.168C>T
ENST00000601003.1:c.52C>T ENSP00000469074.1:p.Pro18Ser
NM_020533.2:c.52C>T NP_065394.1:p.Pro18Ser
NM_020533.3:c.52C>T MANE Select NP_065394.1:p.Pro18Ser