Canonical Allele Identifier: CA347267973

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717332T>A (hg19) ; chr2:g.73490205T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490205T>A , CM000664.2:g.73490205T>A	GRCh38
NC_000002.11:g.73717332T>A , CM000664.1:g.73717332T>A	GRCh37
NC_000002.10:g.73570840T>A	NCBI36
NG_011690.1:g.109453T>A , LRG_741:g.109453T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7865T>A	ENSP00000507671.1:p.Val2622Glu
ENST00000682801.1:c.7865T>A	ENSP00000507862.1:p.Val2622Glu
ENST00000682859.1:c.7865T>A	ENSP00000508222.1:p.Val2622Glu
ENST00000683791.1:c.1257T>A
ENST00000684460.1:c.5317T>A
ENST00000684548.1:c.7865T>A	ENSP00000507421.1:p.Val2622Glu
ENST00000684590.1:c.2312T>A	ENSP00000507376.1:p.Val771Glu
ENST00000684656.1:c.5317T>A
ENST00000613296.6:c.8246T>A MANE Select	ENSP00000482968.1:p.Val2749Glu
ENST00000651434.1:c.896-29570T>A
ENST00000423048.5:c.3030+47T>A	ENSP00000399833.1:n.3030+47T>A
ENST00000484298.5:c.8120T>A	ENSP00000478155.1:p.Val2707Glu
ENST00000613296.4:c.8246T>A	ENSP00000482968.1:p.Val2749Glu
ENST00000614410.4:c.8246T>A	ENSP00000479094.1:p.Val2749Glu
ENST00000620466.4:n.2049T>A
NM_015120.4:c.8249T>A , LRG_741t1:c.8249T>A	NP_055935.4:p.Val2750Glu
NM_001378454.1:c.8246T>A MANE Select	NP_001365383.1:p.Val2749Glu