Canonical Allele Identifier: CA1260981829

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490298C= , CM000664.2:g.73490298C=	GRCh38
NC_000002.11:g.73717425C= , CM000664.1:g.73717425C=	GRCh37
NC_000002.10:g.73570933C=	NCBI36
NG_011690.1:g.109546C= , LRG_741:g.109546C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7958C=	ENSP00000507671.1:p.Ser2653=
ENST00000682801.1:c.7958C=	ENSP00000507862.1:p.Ser2653=
ENST00000682859.1:c.7958C=	ENSP00000508222.1:p.Ser2653=
ENST00000683791.1:c.1350C=
ENST00000684460.1:c.5410C=
ENST00000684548.1:c.7958C=	ENSP00000507421.1:p.Ser2653=
ENST00000684590.1:c.2405C=	ENSP00000507376.1:p.Ser802=
ENST00000684656.1:c.5410C=
ENST00000613296.6:c.8339C= MANE Select	ENSP00000482968.1:p.Ser2780=
ENST00000651434.1:c.896-29477C=
ENST00000423048.5:c.3030+140C=	ENSP00000399833.1:n.3030+140C=
ENST00000484298.5:c.8213C=	ENSP00000478155.1:p.Ser2738=
ENST00000613296.4:c.8339C=	ENSP00000482968.1:p.Ser2780=
ENST00000614410.4:c.8339C=	ENSP00000479094.1:p.Ser2780=
ENST00000620466.4:n.2142C=
NM_015120.4:c.8342C= , LRG_741t1:c.8342C=	NP_055935.4:p.Ser2781=
NM_001378454.1:c.8339C= MANE Select	NP_001365383.1:p.Ser2780=