Canonical Allele Identifier: CA347268296

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717419G>T (hg19) ; chr2:g.73490292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490292G>T , CM000664.2:g.73490292G>T	GRCh38
NC_000002.11:g.73717419G>T , CM000664.1:g.73717419G>T	GRCh37
NC_000002.10:g.73570927G>T	NCBI36
NG_011690.1:g.109540G>T , LRG_741:g.109540G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7952G>T	ENSP00000507671.1:p.Ser2651Ile
ENST00000682801.1:c.7952G>T	ENSP00000507862.1:p.Ser2651Ile
ENST00000682859.1:c.7952G>T	ENSP00000508222.1:p.Ser2651Ile
ENST00000683791.1:c.1344G>T
ENST00000684460.1:c.5404G>T
ENST00000684548.1:c.7952G>T	ENSP00000507421.1:p.Ser2651Ile
ENST00000684590.1:c.2399G>T	ENSP00000507376.1:p.Ser800Ile
ENST00000684656.1:c.5404G>T
ENST00000613296.6:c.8333G>T MANE Select	ENSP00000482968.1:p.Ser2778Ile
ENST00000651434.1:c.896-29483G>T
ENST00000423048.5:c.3030+134G>T	ENSP00000399833.1:n.3030+134G>T
ENST00000484298.5:c.8207G>T	ENSP00000478155.1:p.Ser2736Ile
ENST00000613296.4:c.8333G>T	ENSP00000482968.1:p.Ser2778Ile
ENST00000614410.4:c.8333G>T	ENSP00000479094.1:p.Ser2778Ile
ENST00000620466.4:n.2136G>T
NM_015120.4:c.8336G>T , LRG_741t1:c.8336G>T	NP_055935.4:p.Ser2779Ile
NM_001378454.1:c.8333G>T MANE Select	NP_001365383.1:p.Ser2778Ile