Canonical Allele Identifier: CA403092161

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7598676A>T (hg19) ; chr19:g.7533790A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7533790A>T , CM000681.2:g.7533790A>T	GRCh38
NC_000019.9:g.7598676A>T , CM000681.1:g.7598676A>T	GRCh37
NC_000019.8:g.7504676A>T	NCBI36
NG_013374.1:g.4639A>T
NG_015806.1:g.16181A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1738A>T MANE Select	ENSP00000264079.5:p.Asn580Tyr
ENST00000264079.10:c.1738A>T	ENSP00000264079.5:p.Asn580Tyr
ENST00000394321.9:n.2053A>T
ENST00000599334.1:c.466A>T
ENST00000601870.1:c.91A>T
ENST00000602227.1:n.292A>T
NM_020533.2:c.1738A>T	NP_065394.1:p.Asn580Tyr
NM_020533.3:c.1738A>T MANE Select	NP_065394.1:p.Asn580Tyr