Canonical Allele Identifier: CA2587949559
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7530223-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530223G>T , CM000681.2:g.7530223G>T GRCh38
NC_000019.9:g.7595109G>T , CM000681.1:g.7595109G>T GRCh37
NC_000019.8:g.7501109G>T NCBI36
NG_013374.1:g.1072G>T
NG_015806.1:g.12614G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-63G>T MANE Select ENSP00000264079.5:n.1360-63G>T
ENST00000264079.10:c.1360-63G>T ENSP00000264079.5:n.1360-63G>T
ENST00000394321.9:n.1675-63G>T
ENST00000594692.1:n.356-63G>T
ENST00000595860.5:n.543-63G>T
ENST00000599334.1:c.237-212G>T
NM_020533.2:c.1360-63G>T NP_065394.1:n.1360-63G>T
NM_020533.3:c.1360-63G>T MANE Select NP_065394.1:n.1360-63G>T