Canonical Allele Identifier: CA1260981556

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490142A= , CM000664.2:g.73490142A=	GRCh38
NC_000002.11:g.73717269A= , CM000664.1:g.73717269A=	GRCh37
NC_000002.10:g.73570777A=	NCBI36
NG_011690.1:g.109390A= , LRG_741:g.109390A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7802A=	ENSP00000507671.1:p.Asn2601=
ENST00000682801.1:c.7802A=	ENSP00000507862.1:p.Asn2601=
ENST00000682859.1:c.7802A=	ENSP00000508222.1:p.Asn2601=
ENST00000683791.1:c.1194A=
ENST00000684460.1:c.5254A=
ENST00000684548.1:c.7802A=	ENSP00000507421.1:p.Asn2601=
ENST00000684590.1:c.2249A=	ENSP00000507376.1:p.Asn750=
ENST00000684656.1:c.5254A=
ENST00000613296.6:c.8183A= MANE Select	ENSP00000482968.1:p.Asn2728=
ENST00000651434.1:c.896-29633A=
ENST00000423048.5:c.3014A=	ENSP00000399833.1:p.Asn1005=
ENST00000484298.5:c.8057A=	ENSP00000478155.1:p.Asn2686=
ENST00000613296.4:c.8183A=	ENSP00000482968.1:p.Asn2728=
ENST00000614410.4:c.8183A=	ENSP00000479094.1:p.Asn2728=
ENST00000620466.4:n.1986A=
NM_015120.4:c.8186A= , LRG_741t1:c.8186A=	NP_055935.4:p.Asn2729=
NM_001378454.1:c.8183A= MANE Select	NP_001365383.1:p.Asn2728=