Canonical Allele Identifier: CA347263923

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716807G>T (hg19) ; chr2:g.73489680G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489680G>T , CM000664.2:g.73489680G>T	GRCh38
NC_000002.11:g.73716807G>T , CM000664.1:g.73716807G>T	GRCh37
NC_000002.10:g.73570315G>T	NCBI36
NG_011690.1:g.108928G>T , LRG_741:g.108928G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7340G>T	ENSP00000507671.1:p.Cys2447Phe
ENST00000682801.1:c.7340G>T	ENSP00000507862.1:p.Cys2447Phe
ENST00000682859.1:c.7340G>T	ENSP00000508222.1:p.Cys2447Phe
ENST00000683791.1:c.732G>T
ENST00000684460.1:c.4792G>T
ENST00000684548.1:c.7340G>T	ENSP00000507421.1:p.Cys2447Phe
ENST00000684590.1:c.1787G>T	ENSP00000507376.1:p.Cys596Phe
ENST00000684656.1:c.4792G>T
ENST00000613296.6:c.7721G>T MANE Select	ENSP00000482968.1:p.Cys2574Phe
ENST00000651434.1:c.896-30095G>T
ENST00000423048.5:c.2552G>T	ENSP00000399833.1:p.Cys851Phe
ENST00000484298.5:c.7595G>T	ENSP00000478155.1:p.Cys2532Phe
ENST00000613296.4:c.7721G>T	ENSP00000482968.1:p.Cys2574Phe
ENST00000614410.4:c.7721G>T	ENSP00000479094.1:p.Cys2574Phe
ENST00000620466.4:n.1524G>T
NM_015120.4:c.7724G>T , LRG_741t1:c.7724G>T	NP_055935.4:p.Cys2575Phe
NM_001378454.1:c.7721G>T MANE Select	NP_001365383.1:p.Cys2574Phe