Canonical Allele Identifier: CA993155512
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022635733

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530211_7530223del , CM000681.2:g.7530211_7530223del GRCh38
NC_000019.9:g.7595097_7595109del , CM000681.1:g.7595097_7595109del GRCh37
NC_000019.8:g.7501097_7501109del NCBI36
NG_013374.1:g.1060_1072del
NG_015806.1:g.12602_12614del

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-75_1360-63del MANE Select ENSP00000264079.5:n.1360-75_1360-63del
ENST00000264079.10:c.1360-75_1360-63del ENSP00000264079.5:n.1360-75_1360-63del
ENST00000394321.9:n.1675-75_1675-63del
ENST00000594692.1:n.356-75_356-63del
ENST00000595860.5:n.543-75_543-63del
ENST00000599334.1:c.237-224_237-212del
NM_020533.2:c.1360-75_1360-63del NP_065394.1:n.1360-75_1360-63del
NM_020533.3:c.1360-75_1360-63del MANE Select NP_065394.1:n.1360-75_1360-63del