Canonical Allele Identifier: CA2587946757
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7524912-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524912A>T , CM000681.2:g.7524912A>T GRCh38
NC_000019.9:g.7589798A>T , CM000681.1:g.7589798A>T GRCh37
NC_000019.8:g.7495798A>T NCBI36
NG_015806.1:g.7303A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.32-49A>T MANE Select ENSP00000264079.5:n.32-49A>T
ENST00000264079.10:c.32-49A>T ENSP00000264079.5:n.32-49A>T
ENST00000394321.9:n.112-49A>T
ENST00000596390.1:n.148-49A>T
ENST00000601003.1:c.32-49A>T ENSP00000469074.1:n.32-49A>T
NM_020533.2:c.32-49A>T NP_065394.1:n.32-49A>T
XR_936293.1:n.43T>A
XR_936294.1:n.43T>A
XR_936295.1:n.43T>A
XR_936293.2:n.69T>A
XR_936294.2:n.69T>A
NM_020533.3:c.32-49A>T MANE Select NP_065394.1:n.32-49A>T