Canonical Allele Identifier: CA505232027
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1599252279
gnomAD v4: 19-7525016-A-C
MyVariant Identifiers: chr19:g.7589902A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525016A>C , CM000681.2:g.7525016A>C GRCh38
NC_000019.9:g.7589902A>C , CM000681.1:g.7589902A>C GRCh37
NC_000019.8:g.7495902A>C NCBI36
NG_015806.1:g.7407A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.87A>C MANE Select ENSP00000264079.5:p.Ser29=
ENST00000264079.10:c.87A>C ENSP00000264079.5:p.Ser29=
ENST00000394321.9:n.167A>C
ENST00000596390.1:n.203A>C
ENST00000601003.1:c.87A>C ENSP00000469074.1:p.Ser29=
NM_020533.2:c.87A>C NP_065394.1:p.Ser29=
NM_020533.3:c.87A>C MANE Select NP_065394.1:p.Ser29=
Search 100 bp 5'
Search 100 bp 3'