Canonical Allele Identifier: CA347286391

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799953C>T (hg19) ; chr2:g.73572826C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572826C>T , CM000664.2:g.73572826C>T	GRCh38
NC_000002.11:g.73799953C>T , CM000664.1:g.73799953C>T	GRCh37
NC_000002.10:g.73653461C>T	NCBI36
NG_011690.1:g.192074C>T , LRG_741:g.192074C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10568C>T	ENSP00000507671.1:p.Thr3523Ile
ENST00000682801.1:c.10568C>T	ENSP00000507862.1:p.Thr3523Ile
ENST00000682859.1:c.10568C>T	ENSP00000508222.1:p.Thr3523Ile
ENST00000683791.1:c.3654C>T
ENST00000684460.1:c.7849C>T
ENST00000684548.1:c.10568C>T	ENSP00000507421.1:p.Thr3523Ile
ENST00000684590.1:c.5015C>T	ENSP00000507376.1:p.Thr1672Ile
ENST00000684656.1:c.7894C>T
ENST00000613296.6:c.10949C>T MANE Select	ENSP00000482968.1:p.Thr3650Ile
ENST00000651057.1:c.1103C>T	ENSP00000498504.1:p.Thr368Ile
ENST00000651434.1:c.2305C>T
ENST00000651750.1:c.337C>T
ENST00000652487.1:c.2046C>T
ENST00000423048.5:c.4440C>T	ENSP00000399833.1:n.4440C>T
ENST00000484298.5:c.10823C>T	ENSP00000478155.1:p.Thr3608Ile
ENST00000613296.4:c.10949C>T	ENSP00000482968.1:p.Thr3650Ile
ENST00000614410.4:c.10949C>T	ENSP00000479094.1:p.Thr3650Ile
ENST00000620466.4:n.4752C>T
NM_015120.4:c.10952C>T , LRG_741t1:c.10952C>T	NP_055935.4:p.Thr3651Ile
NM_001378454.1:c.10949C>T MANE Select	NP_001365383.1:p.Thr3650Ile