Canonical Allele Identifier: CA403089657
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7595268C>A (hg19) chr19:g.7530382C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530382C>A , CM000681.2:g.7530382C>A GRCh38
NC_000019.9:g.7595268C>A , CM000681.1:g.7595268C>A GRCh37
NC_000019.8:g.7501268C>A NCBI36
NG_013374.1:g.1231C>A
NG_015806.1:g.12773C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1456C>A MANE Select ENSP00000264079.5:p.Arg486Ser
ENST00000264079.10:c.1456C>A ENSP00000264079.5:p.Arg486Ser
ENST00000394321.9:n.1771C>A
ENST00000594692.1:n.452C>A
ENST00000595860.5:n.639C>A
ENST00000599334.1:c.237-53C>A
NM_020533.2:c.1456C>A NP_065394.1:p.Arg486Ser
NM_020533.3:c.1456C>A MANE Select NP_065394.1:p.Arg486Ser
Search 100 bp 5'
Search 100 bp 3'