Canonical Allele Identifier: CA1260981278

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490009G= , CM000664.2:g.73490009G=	GRCh38
NC_000002.11:g.73717136G= , CM000664.1:g.73717136G=	GRCh37
NC_000002.10:g.73570644G=	NCBI36
NG_011690.1:g.109257G= , LRG_741:g.109257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7669G=	ENSP00000507671.1:p.Val2557=
ENST00000682801.1:c.7669G=	ENSP00000507862.1:p.Val2557=
ENST00000682859.1:c.7669G=	ENSP00000508222.1:p.Val2557=
ENST00000683791.1:c.1061G=
ENST00000684460.1:c.5121G=
ENST00000684548.1:c.7669G=	ENSP00000507421.1:p.Val2557=
ENST00000684590.1:c.2116G=	ENSP00000507376.1:p.Val706=
ENST00000684656.1:c.5121G=
ENST00000613296.6:c.8050G= MANE Select	ENSP00000482968.1:p.Val2684=
ENST00000651434.1:c.896-29766G=
ENST00000423048.5:c.2881G=	ENSP00000399833.1:p.Val961=
ENST00000484298.5:c.7924G=	ENSP00000478155.1:p.Val2642=
ENST00000613296.4:c.8050G=	ENSP00000482968.1:p.Val2684=
ENST00000614410.4:c.8050G=	ENSP00000479094.1:p.Val2684=
ENST00000620466.4:n.1853G=
NM_015120.4:c.8053G= , LRG_741t1:c.8053G=	NP_055935.4:p.Val2685=
NM_001378454.1:c.8050G= MANE Select	NP_001365383.1:p.Val2684=