Canonical Allele Identifier: CA2587948173
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527279_7527295dup , CM000681.2:g.7527279_7527295dup GRCh38
NC_000019.9:g.7592165_7592181dup , CM000681.1:g.7592165_7592181dup GRCh37
NC_000019.8:g.7498165_7498181dup NCBI36
NG_015806.1:g.9670_9686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-241_572-225dup MANE Select ENSP00000264079.5:n.572-241_572-225dup
ENST00000264079.10:c.572-241_572-225dup ENSP00000264079.5:n.572-241_572-225dup
ENST00000394321.9:n.652-241_652-225dup
ENST00000598406.1:n.393-241_393-225dup
ENST00000601003.1:c.571+353_571+369dup ENSP00000469074.1:n.571+353_571+369dup
NM_020533.2:c.572-241_572-225dup NP_065394.1:n.572-241_572-225dup
NM_020533.3:c.572-241_572-225dup MANE Select NP_065394.1:n.572-241_572-225dup