Canonical Allele Identifier: CA403152739
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7589961T>C (hg19) chr19:g.7525075T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525075T>C , CM000681.2:g.7525075T>C GRCh38
NC_000019.9:g.7589961T>C , CM000681.1:g.7589961T>C GRCh37
NC_000019.8:g.7495961T>C NCBI36
NG_015806.1:g.7466T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.146T>C MANE Select ENSP00000264079.5:p.Phe49Ser
ENST00000264079.10:c.146T>C ENSP00000264079.5:p.Phe49Ser
ENST00000394321.9:n.226T>C
ENST00000596390.1:n.262T>C
ENST00000601003.1:c.146T>C ENSP00000469074.1:p.Phe49Ser
NM_020533.2:c.146T>C NP_065394.1:p.Phe49Ser
NM_020533.3:c.146T>C MANE Select NP_065394.1:p.Phe49Ser
Search 100 bp 5'
Search 100 bp 3'