Canonical Allele Identifier: CA403082130
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527564A>T , CM000681.2:g.7527564A>T GRCh38
NC_000019.9:g.7592450A>T , CM000681.1:g.7592450A>T GRCh37
NC_000019.8:g.7498450A>T NCBI36
NG_015806.1:g.9955A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.616A>T MANE Select ENSP00000264079.5:p.Ser206Cys
ENST00000264079.10:c.616A>T ENSP00000264079.5:p.Ser206Cys
ENST00000394321.9:n.696A>T
ENST00000598406.1:n.437A>T
ENST00000601003.1:c.572-300A>T ENSP00000469074.1:n.572-300A>T
NM_020533.2:c.616A>T NP_065394.1:p.Ser206Cys
NM_020533.3:c.616A>T MANE Select NP_065394.1:p.Ser206Cys