Canonical Allele Identifier: CA1714541

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490738C>T , CM000664.2:g.73490738C>T	GRCh38
NC_000002.11:g.73717865C>T , CM000664.1:g.73717865C>T	GRCh37
NC_000002.10:g.73571373C>T	NCBI36
NG_011690.1:g.109986C>T , LRG_741:g.109986C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.8779C>T MANE Select	NP_001365383.1:p.Arg2927Ter
ENST00000613296.6:c.8779C>T MANE Select	ENSP00000482968.1:p.Arg2927Ter
NM_015120.4:c.8782C>T , LRG_741t1:c.8782C>T	NP_055935.4:p.Arg2928Ter
ENST00000423048.5:c.3030+580C>T	ENSP00000399833.1:n.3030+580C>T
ENST00000484298.5:c.8653C>T	ENSP00000478155.1:p.Arg2885Ter
ENST00000613296.4:c.8779C>T	ENSP00000482968.1:p.Arg2927Ter
ENST00000614410.4:c.8779C>T	ENSP00000479094.1:p.Arg2927Ter
ENST00000620466.4:n.2582C>T
ENST00000651434.1:c.896-29037C>T
ENST00000682565.1:c.8398C>T	ENSP00000507671.1:p.Arg2800Ter
ENST00000682801.1:c.8398C>T	ENSP00000507862.1:p.Arg2800Ter
ENST00000682859.1:c.8398C>T	ENSP00000508222.1:p.Arg2800Ter
ENST00000683791.1:c.1790C>T
ENST00000684460.1:c.5850C>T
ENST00000684548.1:c.8398C>T	ENSP00000507421.1:p.Arg2800Ter
ENST00000684590.1:c.2845C>T	ENSP00000507376.1:p.Arg949Ter
ENST00000684656.1:c.5850C>T