Canonical Allele Identifier: CA427001182

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 1161114
• ClinVar RCV Id: RCV001505507
• dbSNP Id: rs920410396
• gnomAD v2: 2-73717306-C-T
• gnomAD v4: 2-73490179-C-T
• MyVariant Identifiers: chr2:g.73717306C>T (hg19) ; chr2:g.73490179C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490179C>T , CM000664.2:g.73490179C>T	GRCh38
NC_000002.11:g.73717306C>T , CM000664.1:g.73717306C>T	GRCh37
NC_000002.10:g.73570814C>T	NCBI36
NG_011690.1:g.109427C>T , LRG_741:g.109427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7839C>T	ENSP00000507671.1:p.Ser2613=
ENST00000682801.1:c.7839C>T	ENSP00000507862.1:p.Ser2613=
ENST00000682859.1:c.7839C>T	ENSP00000508222.1:p.Ser2613=
ENST00000683791.1:c.1231C>T
ENST00000684460.1:c.5291C>T
ENST00000684548.1:c.7839C>T	ENSP00000507421.1:p.Ser2613=
ENST00000684590.1:c.2286C>T	ENSP00000507376.1:p.Ser762=
ENST00000684656.1:c.5291C>T
ENST00000613296.6:c.8220C>T MANE Select	ENSP00000482968.1:p.Ser2740=
ENST00000651434.1:c.896-29596C>T
ENST00000423048.5:c.3030+21C>T	ENSP00000399833.1:n.3030+21C>T
ENST00000484298.5:c.8094C>T	ENSP00000478155.1:p.Ser2698=
ENST00000613296.4:c.8220C>T	ENSP00000482968.1:p.Ser2740=
ENST00000614410.4:c.8220C>T	ENSP00000479094.1:p.Ser2740=
ENST00000620466.4:n.2023C>T
NM_015120.4:c.8223C>T , LRG_741t1:c.8223C>T	NP_055935.4:p.Ser2741=
NM_001378454.1:c.8220C>T MANE Select	NP_001365383.1:p.Ser2740=