Canonical Allele Identifier: CA427024492

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799495C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572368C>T , CM000664.2:g.73572368C>T	GRCh38
NC_000002.11:g.73799495C>T , CM000664.1:g.73799495C>T	GRCh37
NC_000002.10:g.73653003C>T	NCBI36
NG_011690.1:g.191616C>T , LRG_741:g.191616C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10110C>T	ENSP00000507671.1:p.Cys3370=
ENST00000682801.1:c.10110C>T	ENSP00000507862.1:p.Cys3370=
ENST00000682859.1:c.10110C>T	ENSP00000508222.1:p.Cys3370=
ENST00000683791.1:c.3196C>T
ENST00000684460.1:c.7391C>T
ENST00000684548.1:c.10110C>T	ENSP00000507421.1:p.Cys3370=
ENST00000684590.1:c.4557C>T	ENSP00000507376.1:p.Cys1519=
ENST00000684656.1:c.7436C>T
ENST00000613296.6:c.10491C>T MANE Select	ENSP00000482968.1:p.Cys3497=
ENST00000651057.1:c.645C>T	ENSP00000498504.1:p.Cys215=
ENST00000651434.1:c.1847C>T
ENST00000652487.1:c.1588C>T
ENST00000423048.5:c.3982C>T	ENSP00000399833.1:n.3982C>T
ENST00000484298.5:c.10365C>T	ENSP00000478155.1:p.Cys3455=
ENST00000613296.4:c.10491C>T	ENSP00000482968.1:p.Cys3497=
ENST00000614410.4:c.10491C>T	ENSP00000479094.1:p.Cys3497=
ENST00000620466.4:n.4294C>T
NM_015120.4:c.10494C>T , LRG_741t1:c.10494C>T	NP_055935.4:p.Cys3498=
NM_001378454.1:c.10491C>T MANE Select	NP_001365383.1:p.Cys3497=