Canonical Allele Identifier: CA347284175

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 2170177
• ClinVar RCV Id: RCV003085209
• MyVariant Identifiers: chr2:g.73799617C>T (hg19) ; chr2:g.73572490C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572490C>T , CM000664.2:g.73572490C>T	GRCh38
NC_000002.11:g.73799617C>T , CM000664.1:g.73799617C>T	GRCh37
NC_000002.10:g.73653125C>T	NCBI36
NG_011690.1:g.191738C>T , LRG_741:g.191738C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10232C>T	ENSP00000507671.1:p.Thr3411Ile
ENST00000682801.1:c.10232C>T	ENSP00000507862.1:p.Thr3411Ile
ENST00000682859.1:c.10232C>T	ENSP00000508222.1:p.Thr3411Ile
ENST00000683791.1:c.3318C>T
ENST00000684460.1:c.7513C>T
ENST00000684548.1:c.10232C>T	ENSP00000507421.1:p.Thr3411Ile
ENST00000684590.1:c.4679C>T	ENSP00000507376.1:p.Thr1560Ile
ENST00000684656.1:c.7558C>T
ENST00000613296.6:c.10613C>T MANE Select	ENSP00000482968.1:p.Thr3538Ile
ENST00000651057.1:c.767C>T	ENSP00000498504.1:p.Thr256Ile
ENST00000651434.1:c.1969C>T
ENST00000651750.1:c.1C>T
ENST00000652487.1:c.1710C>T
ENST00000423048.5:c.4104C>T	ENSP00000399833.1:n.4104C>T
ENST00000484298.5:c.10487C>T	ENSP00000478155.1:p.Thr3496Ile
ENST00000613296.4:c.10613C>T	ENSP00000482968.1:p.Thr3538Ile
ENST00000614410.4:c.10613C>T	ENSP00000479094.1:p.Thr3538Ile
ENST00000620466.4:n.4416C>T
NM_015120.4:c.10616C>T , LRG_741t1:c.10616C>T	NP_055935.4:p.Thr3539Ile
NM_001378454.1:c.10613C>T MANE Select	NP_001365383.1:p.Thr3538Ile