Canonical Allele Identifier: CA2587946472
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7522788-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7522788G>A , CM000681.2:g.7522788G>A GRCh38
NC_000019.9:g.7587674G>A , CM000681.1:g.7587674G>A GRCh37
NC_000019.8:g.7493674G>A NCBI36
NG_015806.1:g.5179G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.31+7G>A MANE Select ENSP00000264079.5:n.31+7G>A
ENST00000264079.10:c.31+7G>A ENSP00000264079.5:n.31+7G>A
ENST00000394321.9:n.111+7G>A
ENST00000596390.1:n.147+7G>A
ENST00000601003.1:c.31+7G>A ENSP00000469074.1:n.31+7G>A
NM_020533.2:c.31+7G>A NP_065394.1:n.31+7G>A
XR_936293.1:n.926+54C>T
XR_936294.1:n.926+54C>T
XR_936295.1:n.570+54C>T
XR_936293.2:n.952+54C>T
XR_936294.2:n.952+54C>T
NM_020533.3:c.31+7G>A MANE Select NP_065394.1:n.31+7G>A