Canonical Allele Identifier: CA403081142
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526762A>C , CM000681.2:g.7526762A>C GRCh38
NC_000019.9:g.7591648A>C , CM000681.1:g.7591648A>C GRCh37
NC_000019.8:g.7497648A>C NCBI36
NG_015806.1:g.9153A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.407A>C MANE Select ENSP00000264079.5:p.Tyr136Ser
ENST00000264079.10:c.407A>C ENSP00000264079.5:p.Tyr136Ser
ENST00000394321.9:n.487A>C
ENST00000596008.1:n.369A>C
ENST00000598406.1:n.228A>C
ENST00000601003.1:c.407A>C ENSP00000469074.1:p.Tyr136Ser
NM_020533.2:c.407A>C NP_065394.1:p.Tyr136Ser
NM_020533.3:c.407A>C MANE Select NP_065394.1:p.Tyr136Ser