Canonical Allele Identifier: CA403087480

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7594512G>T (hg19) ; chr19:g.7529626G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7529626G>T , CM000681.2:g.7529626G>T	GRCh38
NC_000019.9:g.7594512G>T , CM000681.1:g.7594512G>T	GRCh37
NC_000019.8:g.7500512G>T	NCBI36
NG_013374.1:g.475G>T
NG_015806.1:g.12017G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1273G>T MANE Select	ENSP00000264079.5:p.Val425Phe
ENST00000264079.10:c.1273G>T	ENSP00000264079.5:p.Val425Phe
ENST00000394321.9:n.1588G>T
ENST00000594692.1:n.269G>T
ENST00000595860.5:n.456G>T
ENST00000599334.1:c.150G>T
NM_020533.2:c.1273G>T	NP_065394.1:p.Val425Phe
NM_020533.3:c.1273G>T MANE Select	NP_065394.1:p.Val425Phe