Canonical Allele Identifier: CA347266643

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717052A>G (hg19) ; chr2:g.73489925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489925A>G , CM000664.2:g.73489925A>G	GRCh38
NC_000002.11:g.73717052A>G , CM000664.1:g.73717052A>G	GRCh37
NC_000002.10:g.73570560A>G	NCBI36
NG_011690.1:g.109173A>G , LRG_741:g.109173A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7585A>G	ENSP00000507671.1:p.Asn2529Asp
ENST00000682801.1:c.7585A>G	ENSP00000507862.1:p.Asn2529Asp
ENST00000682859.1:c.7585A>G	ENSP00000508222.1:p.Asn2529Asp
ENST00000683791.1:c.977A>G
ENST00000684460.1:c.5037A>G
ENST00000684548.1:c.7585A>G	ENSP00000507421.1:p.Asn2529Asp
ENST00000684590.1:c.2032A>G	ENSP00000507376.1:p.Asn678Asp
ENST00000684656.1:c.5037A>G
ENST00000613296.6:c.7966A>G MANE Select	ENSP00000482968.1:p.Asn2656Asp
ENST00000651434.1:c.896-29850A>G
ENST00000423048.5:c.2797A>G	ENSP00000399833.1:p.Asn933Asp
ENST00000484298.5:c.7840A>G	ENSP00000478155.1:p.Asn2614Asp
ENST00000613296.4:c.7966A>G	ENSP00000482968.1:p.Asn2656Asp
ENST00000614410.4:c.7966A>G	ENSP00000479094.1:p.Asn2656Asp
ENST00000620466.4:n.1769A>G
NM_015120.4:c.7969A>G , LRG_741t1:c.7969A>G	NP_055935.4:p.Asn2657Asp
NM_001378454.1:c.7966A>G MANE Select	NP_001365383.1:p.Asn2656Asp