Canonical Allele Identifier: CA2587948035
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527124-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527124T>G , CM000681.2:g.7527124T>G GRCh38
NC_000019.9:g.7592010T>G , CM000681.1:g.7592010T>G GRCh37
NC_000019.8:g.7498010T>G NCBI36
NG_015806.1:g.9515T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.571+198T>G MANE Select ENSP00000264079.5:n.571+198T>G
ENST00000264079.10:c.571+198T>G ENSP00000264079.5:n.571+198T>G
ENST00000394321.9:n.651+198T>G
ENST00000596008.1:n.731T>G
ENST00000598406.1:n.392+198T>G
ENST00000601003.1:c.571+198T>G ENSP00000469074.1:n.571+198T>G
NM_020533.2:c.571+198T>G NP_065394.1:n.571+198T>G
NM_020533.3:c.571+198T>G MANE Select NP_065394.1:n.571+198T>G