Canonical Allele Identifier: CA403081164
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022576439
gnomAD v4: 19-7526767-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526767G>T , CM000681.2:g.7526767G>T GRCh38
NC_000019.9:g.7591653G>T , CM000681.1:g.7591653G>T GRCh37
NC_000019.8:g.7497653G>T NCBI36
NG_015806.1:g.9158G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.412G>T MANE Select ENSP00000264079.5:p.Ala138Ser
ENST00000264079.10:c.412G>T ENSP00000264079.5:p.Ala138Ser
ENST00000394321.9:n.492G>T
ENST00000596008.1:n.374G>T
ENST00000598406.1:n.233G>T
ENST00000601003.1:c.412G>T ENSP00000469074.1:p.Ala138Ser
NM_020533.2:c.412G>T NP_065394.1:p.Ala138Ser
NM_020533.3:c.412G>T MANE Select NP_065394.1:p.Ala138Ser