Canonical Allele Identifier: CA427000779

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717168G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490041G>T , CM000664.2:g.73490041G>T	GRCh38
NC_000002.11:g.73717168G>T , CM000664.1:g.73717168G>T	GRCh37
NC_000002.10:g.73570676G>T	NCBI36
NG_011690.1:g.109289G>T , LRG_741:g.109289G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7701G>T	ENSP00000507671.1:p.Val2567=
ENST00000682801.1:c.7701G>T	ENSP00000507862.1:p.Val2567=
ENST00000682859.1:c.7701G>T	ENSP00000508222.1:p.Val2567=
ENST00000683791.1:c.1093G>T
ENST00000684460.1:c.5153G>T
ENST00000684548.1:c.7701G>T	ENSP00000507421.1:p.Val2567=
ENST00000684590.1:c.2148G>T	ENSP00000507376.1:p.Val716=
ENST00000684656.1:c.5153G>T
ENST00000613296.6:c.8082G>T MANE Select	ENSP00000482968.1:p.Val2694=
ENST00000651434.1:c.896-29734G>T
ENST00000423048.5:c.2913G>T	ENSP00000399833.1:p.Val971=
ENST00000484298.5:c.7956G>T	ENSP00000478155.1:p.Val2652=
ENST00000613296.4:c.8082G>T	ENSP00000482968.1:p.Val2694=
ENST00000614410.4:c.8082G>T	ENSP00000479094.1:p.Val2694=
ENST00000620466.4:n.1885G>T
NM_015120.4:c.8085G>T , LRG_741t1:c.8085G>T	NP_055935.4:p.Val2695=
NM_001378454.1:c.8082G>T MANE Select	NP_001365383.1:p.Val2694=