Canonical Allele Identifier: CA426783628

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828534C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601407C>T , CM000664.2:g.73601407C>T	GRCh38
NC_000002.11:g.73828534C>T , CM000664.1:g.73828534C>T	GRCh37
NC_000002.10:g.73682042C>T	NCBI36
NG_011690.1:g.220655C>T , LRG_741:g.220655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11704C>T	ENSP00000507671.1:p.Leu3902=
ENST00000682801.1:c.11167-778C>T	ENSP00000507862.1:n.11167-778C>T
ENST00000682859.1:c.11704C>T	ENSP00000508222.1:p.Leu3902=
ENST00000683791.1:c.4790C>T
ENST00000684460.1:c.8985C>T
ENST00000684548.1:c.11704C>T	ENSP00000507421.1:p.Leu3902=
ENST00000684590.1:c.6151C>T	ENSP00000507376.1:p.Leu2051=
ENST00000684656.1:c.9169C>T
ENST00000613296.6:c.12085C>T MANE Select	ENSP00000482968.1:p.Leu4029=
ENST00000651057.1:c.2239C>T	ENSP00000498504.1:p.Leu747=
ENST00000651434.1:c.3441C>T
ENST00000651750.1:c.1260+526C>T
ENST00000652487.1:c.3256C>T
ENST00000464408.3:n.260C>T
ENST00000484298.5:c.11959C>T	ENSP00000478155.1:p.Leu3987=
ENST00000613296.4:c.12085C>T	ENSP00000482968.1:p.Leu4029=
ENST00000620466.4:n.5888C>T
NM_015120.4:c.12088C>T , LRG_741t1:c.12088C>T	NP_055935.4:p.Leu4030=
NM_001378454.1:c.12085C>T MANE Select	NP_001365383.1:p.Leu4029=