Canonical Allele Identifier: CA347283346

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799521T>A (hg19) ; chr2:g.73572394T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572394T>A , CM000664.2:g.73572394T>A	GRCh38
NC_000002.11:g.73799521T>A , CM000664.1:g.73799521T>A	GRCh37
NC_000002.10:g.73653029T>A	NCBI36
NG_011690.1:g.191642T>A , LRG_741:g.191642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10136T>A	ENSP00000507671.1:p.Phe3379Tyr
ENST00000682801.1:c.10136T>A	ENSP00000507862.1:p.Phe3379Tyr
ENST00000682859.1:c.10136T>A	ENSP00000508222.1:p.Phe3379Tyr
ENST00000683791.1:c.3222T>A
ENST00000684460.1:c.7417T>A
ENST00000684548.1:c.10136T>A	ENSP00000507421.1:p.Phe3379Tyr
ENST00000684590.1:c.4583T>A	ENSP00000507376.1:p.Phe1528Tyr
ENST00000684656.1:c.7462T>A
ENST00000613296.6:c.10517T>A MANE Select	ENSP00000482968.1:p.Phe3506Tyr
ENST00000651057.1:c.671T>A	ENSP00000498504.1:p.Phe224Tyr
ENST00000651434.1:c.1873T>A
ENST00000652487.1:c.1614T>A
ENST00000423048.5:c.4008T>A	ENSP00000399833.1:n.4008T>A
ENST00000484298.5:c.10391T>A	ENSP00000478155.1:p.Phe3464Tyr
ENST00000613296.4:c.10517T>A	ENSP00000482968.1:p.Phe3506Tyr
ENST00000614410.4:c.10517T>A	ENSP00000479094.1:p.Phe3506Tyr
ENST00000620466.4:n.4320T>A
NM_015120.4:c.10520T>A , LRG_741t1:c.10520T>A	NP_055935.4:p.Phe3507Tyr
NM_001378454.1:c.10517T>A MANE Select	NP_001365383.1:p.Phe3506Tyr