Canonical Allele Identifier: CA631318865
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1390123853
gnomAD v2: 19-7595118-C-T
gnomAD v3: 19-7530232-C-T
gnomAD v4: 19-7530232-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530232C>T , CM000681.2:g.7530232C>T GRCh38
NC_000019.9:g.7595118C>T , CM000681.1:g.7595118C>T GRCh37
NC_000019.8:g.7501118C>T NCBI36
NG_013374.1:g.1081C>T
NG_015806.1:g.12623C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-54C>T MANE Select ENSP00000264079.5:n.1360-54C>T
ENST00000264079.10:c.1360-54C>T ENSP00000264079.5:n.1360-54C>T
ENST00000394321.9:n.1675-54C>T
ENST00000594692.1:n.356-54C>T
ENST00000595860.5:n.543-54C>T
ENST00000599334.1:c.237-203C>T
NM_020533.2:c.1360-54C>T NP_065394.1:n.1360-54C>T
NM_020533.3:c.1360-54C>T MANE Select NP_065394.1:n.1360-54C>T