Canonical Allele Identifier: CA2739637916
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527785A>T , CM000681.2:g.7527785A>T GRCh38
NC_000019.9:g.7592671A>T , CM000681.1:g.7592671A>T GRCh37
NC_000019.8:g.7498671A>T NCBI36
NG_015806.1:g.10176A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.681-79A>T MANE Select ENSP00000264079.5:n.681-79A>T
ENST00000264079.10:c.681-79A>T ENSP00000264079.5:n.681-79A>T
ENST00000394321.9:n.917A>T
ENST00000601003.1:c.572-79A>T ENSP00000469074.1:n.572-79A>T
NM_020533.2:c.681-79A>T NP_065394.1:n.681-79A>T
NM_020533.3:c.681-79A>T MANE Select NP_065394.1:n.681-79A>T