Canonical Allele Identifier: CA427024580

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799822G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572695G>T , CM000664.2:g.73572695G>T	GRCh38
NC_000002.11:g.73799822G>T , CM000664.1:g.73799822G>T	GRCh37
NC_000002.10:g.73653330G>T	NCBI36
NG_011690.1:g.191943G>T , LRG_741:g.191943G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10437G>T	ENSP00000507671.1:p.Arg3479=
ENST00000682801.1:c.10437G>T	ENSP00000507862.1:p.Arg3479=
ENST00000682859.1:c.10437G>T	ENSP00000508222.1:p.Arg3479=
ENST00000683791.1:c.3523G>T
ENST00000684460.1:c.7718G>T
ENST00000684548.1:c.10437G>T	ENSP00000507421.1:p.Arg3479=
ENST00000684590.1:c.4884G>T	ENSP00000507376.1:p.Arg1628=
ENST00000684656.1:c.7763G>T
ENST00000613296.6:c.10818G>T MANE Select	ENSP00000482968.1:p.Arg3606=
ENST00000651057.1:c.972G>T	ENSP00000498504.1:p.Arg324=
ENST00000651434.1:c.2174G>T
ENST00000651750.1:c.206G>T
ENST00000652487.1:c.1915G>T
ENST00000423048.5:c.4309G>T	ENSP00000399833.1:n.4309G>T
ENST00000484298.5:c.10692G>T	ENSP00000478155.1:p.Arg3564=
ENST00000613296.4:c.10818G>T	ENSP00000482968.1:p.Arg3606=
ENST00000614410.4:c.10818G>T	ENSP00000479094.1:p.Arg3606=
ENST00000620466.4:n.4621G>T
NM_015120.4:c.10821G>T , LRG_741t1:c.10821G>T	NP_055935.4:p.Arg3607=
NM_001378454.1:c.10818G>T MANE Select	NP_001365383.1:p.Arg3606=