Canonical Allele Identifier: CA403083677
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7592755T>A (hg19) chr19:g.7527869T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527869T>A , CM000681.2:g.7527869T>A GRCh38
NC_000019.9:g.7592755T>A , CM000681.1:g.7592755T>A GRCh37
NC_000019.8:g.7498755T>A NCBI36
NG_015806.1:g.10260T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.686T>A MANE Select ENSP00000264079.5:p.Val229Asp
ENST00000264079.10:c.686T>A ENSP00000264079.5:p.Val229Asp
ENST00000394321.9:n.1001T>A
ENST00000601003.1:c.577T>A ENSP00000469074.1:p.Ser193Thr
NM_020533.2:c.686T>A NP_065394.1:p.Val229Asp
NM_020533.3:c.686T>A MANE Select NP_065394.1:p.Val229Asp
Search 100 bp 5'
Search 100 bp 3'