Canonical Allele Identifier: CA347268986

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 3010495
• ClinVar RCV Id: RCV003862134
• MyVariant Identifiers: chr2:g.73717548A>T (hg19) ; chr2:g.73490421A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490421A>T , CM000664.2:g.73490421A>T	GRCh38
NC_000002.11:g.73717548A>T , CM000664.1:g.73717548A>T	GRCh37
NC_000002.10:g.73571056A>T	NCBI36
NG_011690.1:g.109669A>T , LRG_741:g.109669A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.8081A>T	ENSP00000507671.1:p.His2694Leu
ENST00000682801.1:c.8081A>T	ENSP00000507862.1:p.His2694Leu
ENST00000682859.1:c.8081A>T	ENSP00000508222.1:p.His2694Leu
ENST00000683791.1:c.1473A>T
ENST00000684460.1:c.5533A>T
ENST00000684548.1:c.8081A>T	ENSP00000507421.1:p.His2694Leu
ENST00000684590.1:c.2528A>T	ENSP00000507376.1:p.His843Leu
ENST00000684656.1:c.5533A>T
ENST00000613296.6:c.8462A>T MANE Select	ENSP00000482968.1:p.His2821Leu
ENST00000651434.1:c.896-29354A>T
ENST00000423048.5:c.3030+263A>T	ENSP00000399833.1:n.3030+263A>T
ENST00000484298.5:c.8336A>T	ENSP00000478155.1:p.His2779Leu
ENST00000613296.4:c.8462A>T	ENSP00000482968.1:p.His2821Leu
ENST00000614410.4:c.8462A>T	ENSP00000479094.1:p.His2821Leu
ENST00000620466.4:n.2265A>T
NM_015120.4:c.8465A>T , LRG_741t1:c.8465A>T	NP_055935.4:p.His2822Leu
NM_001378454.1:c.8462A>T MANE Select	NP_001365383.1:p.His2821Leu