Canonical Allele Identifier: CA347264035

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716858C>T (hg19) ; chr2:g.73489731C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489731C>T , CM000664.2:g.73489731C>T	GRCh38
NC_000002.11:g.73716858C>T , CM000664.1:g.73716858C>T	GRCh37
NC_000002.10:g.73570366C>T	NCBI36
NG_011690.1:g.108979C>T , LRG_741:g.108979C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7391C>T	ENSP00000507671.1:p.Thr2464Ile
ENST00000682801.1:c.7391C>T	ENSP00000507862.1:p.Thr2464Ile
ENST00000682859.1:c.7391C>T	ENSP00000508222.1:p.Thr2464Ile
ENST00000683791.1:c.783C>T
ENST00000684460.1:c.4843C>T
ENST00000684548.1:c.7391C>T	ENSP00000507421.1:p.Thr2464Ile
ENST00000684590.1:c.1838C>T	ENSP00000507376.1:p.Thr613Ile
ENST00000684656.1:c.4843C>T
ENST00000613296.6:c.7772C>T MANE Select	ENSP00000482968.1:p.Thr2591Ile
ENST00000651434.1:c.896-30044C>T
ENST00000423048.5:c.2603C>T	ENSP00000399833.1:p.Thr868Ile
ENST00000484298.5:c.7646C>T	ENSP00000478155.1:p.Thr2549Ile
ENST00000613296.4:c.7772C>T	ENSP00000482968.1:p.Thr2591Ile
ENST00000614410.4:c.7772C>T	ENSP00000479094.1:p.Thr2591Ile
ENST00000620466.4:n.1575C>T
NM_015120.4:c.7775C>T , LRG_741t1:c.7775C>T	NP_055935.4:p.Thr2592Ile
NM_001378454.1:c.7772C>T MANE Select	NP_001365383.1:p.Thr2591Ile