Canonical Allele Identifier: CA403082384
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7592491G>C (hg19) chr19:g.7527605G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527605G>C , CM000681.2:g.7527605G>C GRCh38
NC_000019.9:g.7592491G>C , CM000681.1:g.7592491G>C GRCh37
NC_000019.8:g.7498491G>C NCBI36
NG_015806.1:g.9996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.657G>C MANE Select ENSP00000264079.5:p.Lys219Asn
ENST00000264079.10:c.657G>C ENSP00000264079.5:p.Lys219Asn
ENST00000394321.9:n.737G>C
ENST00000598406.1:n.478G>C
ENST00000601003.1:c.572-259G>C ENSP00000469074.1:n.572-259G>C
NM_020533.2:c.657G>C NP_065394.1:p.Lys219Asn
NM_020533.3:c.657G>C MANE Select NP_065394.1:p.Lys219Asn
Search 100 bp 5'
Search 100 bp 3'