Canonical Allele Identifier: CA347285999

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799883G>T (hg19) ; chr2:g.73572756G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572756G>T , CM000664.2:g.73572756G>T	GRCh38
NC_000002.11:g.73799883G>T , CM000664.1:g.73799883G>T	GRCh37
NC_000002.10:g.73653391G>T	NCBI36
NG_011690.1:g.192004G>T , LRG_741:g.192004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10498G>T	ENSP00000507671.1:p.Asp3500Tyr
ENST00000682801.1:c.10498G>T	ENSP00000507862.1:p.Asp3500Tyr
ENST00000682859.1:c.10498G>T	ENSP00000508222.1:p.Asp3500Tyr
ENST00000683791.1:c.3584G>T
ENST00000684460.1:c.7779G>T
ENST00000684548.1:c.10498G>T	ENSP00000507421.1:p.Asp3500Tyr
ENST00000684590.1:c.4945G>T	ENSP00000507376.1:p.Asp1649Tyr
ENST00000684656.1:c.7824G>T
ENST00000613296.6:c.10879G>T MANE Select	ENSP00000482968.1:p.Asp3627Tyr
ENST00000651057.1:c.1033G>T	ENSP00000498504.1:p.Asp345Tyr
ENST00000651434.1:c.2235G>T
ENST00000651750.1:c.267G>T
ENST00000652487.1:c.1976G>T
ENST00000423048.5:c.4370G>T	ENSP00000399833.1:n.4370G>T
ENST00000484298.5:c.10753G>T	ENSP00000478155.1:p.Asp3585Tyr
ENST00000613296.4:c.10879G>T	ENSP00000482968.1:p.Asp3627Tyr
ENST00000614410.4:c.10879G>T	ENSP00000479094.1:p.Asp3627Tyr
ENST00000620466.4:n.4682G>T
NM_015120.4:c.10882G>T , LRG_741t1:c.10882G>T	NP_055935.4:p.Asp3628Tyr
NM_001378454.1:c.10879G>T MANE Select	NP_001365383.1:p.Asp3627Tyr