Canonical Allele Identifier: CA2576596969
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527492A>T , CM000681.2:g.7527492A>T GRCh38
NC_000019.9:g.7592378A>T , CM000681.1:g.7592378A>T GRCh37
NC_000019.8:g.7498378A>T NCBI36
NG_015806.1:g.9883A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-28A>T MANE Select ENSP00000264079.5:n.572-28A>T
ENST00000264079.10:c.572-28A>T ENSP00000264079.5:n.572-28A>T
ENST00000394321.9:n.652-28A>T
ENST00000598406.1:n.393-28A>T
ENST00000601003.1:c.572-372A>T ENSP00000469074.1:n.572-372A>T
NM_020533.2:c.572-28A>T NP_065394.1:n.572-28A>T
NM_020533.3:c.572-28A>T MANE Select NP_065394.1:n.572-28A>T