Canonical Allele Identifier: CA1261033966

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601364G= , CM000664.2:g.73601364G=	GRCh38
NC_000002.11:g.73828491G= , CM000664.1:g.73828491G=	GRCh37
NC_000002.10:g.73681999G=	NCBI36
NG_011690.1:g.220612G= , LRG_741:g.220612G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11661G=	ENSP00000507671.1:p.Arg3887=
ENST00000682801.1:c.11167-821G=	ENSP00000507862.1:n.11167-821G=
ENST00000682859.1:c.11661G=	ENSP00000508222.1:p.Arg3887=
ENST00000683791.1:c.4747G=
ENST00000684460.1:c.8942G=
ENST00000684548.1:c.11661G=	ENSP00000507421.1:p.Arg3887=
ENST00000684590.1:c.6108G=	ENSP00000507376.1:p.Arg2036=
ENST00000684656.1:c.9126G=
ENST00000613296.6:c.12042G= MANE Select	ENSP00000482968.1:p.Arg4014=
ENST00000651057.1:c.2196G=	ENSP00000498504.1:p.Arg732=
ENST00000651434.1:c.3398G=
ENST00000651750.1:c.1260+483G=
ENST00000652487.1:c.3213G=
ENST00000464408.3:n.217G=
ENST00000484298.5:c.11916G=	ENSP00000478155.1:p.Arg3972=
ENST00000613296.4:c.12042G=	ENSP00000482968.1:p.Arg4014=
ENST00000620466.4:n.5845G=
NM_015120.4:c.12045G= , LRG_741t1:c.12045G=	NP_055935.4:p.Arg4015=
NM_001378454.1:c.12042G= MANE Select	NP_001365383.1:p.Arg4014=