Canonical Allele Identifier: CA347264025

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716852C>T (hg19) ; chr2:g.73489725C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489725C>T , CM000664.2:g.73489725C>T	GRCh38
NC_000002.11:g.73716852C>T , CM000664.1:g.73716852C>T	GRCh37
NC_000002.10:g.73570360C>T	NCBI36
NG_011690.1:g.108973C>T , LRG_741:g.108973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7385C>T	ENSP00000507671.1:p.Thr2462Ile
ENST00000682801.1:c.7385C>T	ENSP00000507862.1:p.Thr2462Ile
ENST00000682859.1:c.7385C>T	ENSP00000508222.1:p.Thr2462Ile
ENST00000683791.1:c.777C>T
ENST00000684460.1:c.4837C>T
ENST00000684548.1:c.7385C>T	ENSP00000507421.1:p.Thr2462Ile
ENST00000684590.1:c.1832C>T	ENSP00000507376.1:p.Thr611Ile
ENST00000684656.1:c.4837C>T
ENST00000613296.6:c.7766C>T MANE Select	ENSP00000482968.1:p.Thr2589Ile
ENST00000651434.1:c.896-30050C>T
ENST00000423048.5:c.2597C>T	ENSP00000399833.1:p.Thr866Ile
ENST00000484298.5:c.7640C>T	ENSP00000478155.1:p.Thr2547Ile
ENST00000613296.4:c.7766C>T	ENSP00000482968.1:p.Thr2589Ile
ENST00000614410.4:c.7766C>T	ENSP00000479094.1:p.Thr2589Ile
ENST00000620466.4:n.1569C>T
NM_015120.4:c.7769C>T , LRG_741t1:c.7769C>T	NP_055935.4:p.Thr2590Ile
NM_001378454.1:c.7766C>T MANE Select	NP_001365383.1:p.Thr2589Ile