Canonical Allele Identifier: CA1032214265
Gene: ALMS1 HGNC NCBI

Linked Data

dbSNP Id: rs1674942017

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73572158_73572159del , CM000664.2:g.73572158_73572159del GRCh38
NC_000002.11:g.73799285_73799286del , CM000664.1:g.73799285_73799286del GRCh37
NC_000002.10:g.73652793_73652794del NCBI36
NG_011690.1:g.191406_191407del , LRG_741:g.191406_191407del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682565.1:c.10004-104_10004-103del ENSP00000507671.1:n.10004-104_10004-103del
ENST00000682801.1:c.10004-104_10004-103del ENSP00000507862.1:n.10004-104_10004-103del
ENST00000682859.1:c.10004-104_10004-103del ENSP00000508222.1:n.10004-104_10004-103del
ENST00000683791.1:c.3090-104_3090-103del
ENST00000684460.1:c.7285-104_7285-103del
ENST00000684548.1:c.10004-104_10004-103del ENSP00000507421.1:n.10004-104_10004-103del
ENST00000684590.1:c.4451-104_4451-103del ENSP00000507376.1:n.4451-104_4451-103del
ENST00000684656.1:c.7330-104_7330-103del
ENST00000613296.6:c.10385-104_10385-103del MANE Select ENSP00000482968.1:n.10385-104_10385-103del
ENST00000651057.1:c.539-104_539-103del ENSP00000498504.1:n.539-104_539-103del
ENST00000651434.1:c.1741-104_1741-103del
ENST00000652487.1:c.1482-104_1482-103del
ENST00000423048.5:c.3876-104_3876-103del ENSP00000399833.1:n.3876-104_3876-103del
ENST00000484298.5:c.10259-104_10259-103del ENSP00000478155.1:n.10259-104_10259-103del
ENST00000613296.4:c.10385-104_10385-103del ENSP00000482968.1:n.10385-104_10385-103del
ENST00000614410.4:c.10385-104_10385-103del ENSP00000479094.1:n.10385-104_10385-103del
ENST00000620466.4:n.4188-104_4188-103del
NM_015120.4:c.10388-104_10388-103del , LRG_741t1:c.10388-104_10388-103del NP_055935.4:n.10388-104_10388-103del
NM_001378454.1:c.10385-104_10385-103del MANE Select NP_001365383.1:n.10385-104_10385-103del