Canonical Allele Identifier: CA9139142
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2305888
gnomAD v2: 19-7595159-G-T
gnomAD v4: 19-7530273-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530273G>T , CM000681.2:g.7530273G>T GRCh38
NC_000019.9:g.7595159G>T , CM000681.1:g.7595159G>T GRCh37
NC_000019.8:g.7501159G>T NCBI36
NG_013374.1:g.1122G>T
NG_015806.1:g.12664G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-13G>T MANE Select ENSP00000264079.5:n.1360-13G>T
ENST00000264079.10:c.1360-13G>T ENSP00000264079.5:n.1360-13G>T
ENST00000394321.9:n.1675-13G>T
ENST00000594692.1:n.356-13G>T
ENST00000595860.5:n.543-13G>T
ENST00000599334.1:c.237-162G>T
NM_020533.2:c.1360-13G>T NP_065394.1:n.1360-13G>T
NM_020533.3:c.1360-13G>T MANE Select NP_065394.1:n.1360-13G>T