Canonical Allele Identifier: CA505232321

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7595186C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7530300C>T , CM000681.2:g.7530300C>T	GRCh38
NC_000019.9:g.7595186C>T , CM000681.1:g.7595186C>T	GRCh37
NC_000019.8:g.7501186C>T	NCBI36
NG_013374.1:g.1149C>T
NG_015806.1:g.12691C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1374C>T MANE Select	ENSP00000264079.5:p.Ser458=
ENST00000264079.10:c.1374C>T	ENSP00000264079.5:p.Ser458=
ENST00000394321.9:n.1689C>T
ENST00000594692.1:n.370C>T
ENST00000595860.5:n.557C>T
ENST00000599334.1:c.237-135C>T
NM_020533.2:c.1374C>T	NP_065394.1:p.Ser458=
NM_020533.3:c.1374C>T MANE Select	NP_065394.1:p.Ser458=