Canonical Allele Identifier: CA2320961990
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526827_7526829delinsACC , CM000681.2:g.7526827_7526829delinsACC GRCh38
NC_000019.9:g.7591713_7591715delinsACC , CM000681.1:g.7591713_7591715delinsACC GRCh37
NC_000019.8:g.7497713_7497715delinsACC NCBI36
NG_015806.1:g.9218_9220delinsACC

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.472_474delinsACC MANE Select ENSP00000264079.5:p.Thr158=
ENST00000264079.10:c.472_474delinsACC ENSP00000264079.5:p.Thr158=
ENST00000394321.9:n.552_554delinsACC
ENST00000596008.1:n.434_436delinsACC
ENST00000598406.1:n.293_295delinsACC
ENST00000601003.1:c.472_474delinsACC ENSP00000469074.1:p.Thr158=
NM_020533.2:c.472_474delinsACC NP_065394.1:p.Thr158=
NM_020533.3:c.472_474delinsACC MANE Select NP_065394.1:p.Thr158=