Canonical Allele Identifier: CA403152365
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524982C>T , CM000681.2:g.7524982C>T GRCh38
NC_000019.9:g.7589868C>T , CM000681.1:g.7589868C>T GRCh37
NC_000019.8:g.7495868C>T NCBI36
NG_015806.1:g.7373C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.53C>T MANE Select ENSP00000264079.5:p.Pro18Leu
ENST00000264079.10:c.53C>T ENSP00000264079.5:p.Pro18Leu
ENST00000394321.9:n.133C>T
ENST00000596390.1:n.169C>T
ENST00000601003.1:c.53C>T ENSP00000469074.1:p.Pro18Leu
NM_020533.2:c.53C>T NP_065394.1:p.Pro18Leu
NM_020533.3:c.53C>T MANE Select NP_065394.1:p.Pro18Leu