Canonical Allele Identifier: CA427000714

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717060A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489933A>T , CM000664.2:g.73489933A>T	GRCh38
NC_000002.11:g.73717060A>T , CM000664.1:g.73717060A>T	GRCh37
NC_000002.10:g.73570568A>T	NCBI36
NG_011690.1:g.109181A>T , LRG_741:g.109181A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7593A>T	ENSP00000507671.1:p.Ile2531=
ENST00000682801.1:c.7593A>T	ENSP00000507862.1:p.Ile2531=
ENST00000682859.1:c.7593A>T	ENSP00000508222.1:p.Ile2531=
ENST00000683791.1:c.985A>T
ENST00000684460.1:c.5045A>T
ENST00000684548.1:c.7593A>T	ENSP00000507421.1:p.Ile2531=
ENST00000684590.1:c.2040A>T	ENSP00000507376.1:p.Ile680=
ENST00000684656.1:c.5045A>T
ENST00000613296.6:c.7974A>T MANE Select	ENSP00000482968.1:p.Ile2658=
ENST00000651434.1:c.896-29842A>T
ENST00000423048.5:c.2805A>T	ENSP00000399833.1:p.Ile935=
ENST00000484298.5:c.7848A>T	ENSP00000478155.1:p.Ile2616=
ENST00000613296.4:c.7974A>T	ENSP00000482968.1:p.Ile2658=
ENST00000614410.4:c.7974A>T	ENSP00000479094.1:p.Ile2658=
ENST00000620466.4:n.1777A>T
NM_015120.4:c.7977A>T , LRG_741t1:c.7977A>T	NP_055935.4:p.Ile2659=
NM_001378454.1:c.7974A>T MANE Select	NP_001365383.1:p.Ile2658=