Canonical Allele Identifier: CA427001226

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717321A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490194A>T , CM000664.2:g.73490194A>T	GRCh38
NC_000002.11:g.73717321A>T , CM000664.1:g.73717321A>T	GRCh37
NC_000002.10:g.73570829A>T	NCBI36
NG_011690.1:g.109442A>T , LRG_741:g.109442A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7854A>T	ENSP00000507671.1:p.Ala2618=
ENST00000682801.1:c.7854A>T	ENSP00000507862.1:p.Ala2618=
ENST00000682859.1:c.7854A>T	ENSP00000508222.1:p.Ala2618=
ENST00000683791.1:c.1246A>T
ENST00000684460.1:c.5306A>T
ENST00000684548.1:c.7854A>T	ENSP00000507421.1:p.Ala2618=
ENST00000684590.1:c.2301A>T	ENSP00000507376.1:p.Ala767=
ENST00000684656.1:c.5306A>T
ENST00000613296.6:c.8235A>T MANE Select	ENSP00000482968.1:p.Ala2745=
ENST00000651434.1:c.896-29581A>T
ENST00000423048.5:c.3030+36A>T	ENSP00000399833.1:n.3030+36A>T
ENST00000484298.5:c.8109A>T	ENSP00000478155.1:p.Ala2703=
ENST00000613296.4:c.8235A>T	ENSP00000482968.1:p.Ala2745=
ENST00000614410.4:c.8235A>T	ENSP00000479094.1:p.Ala2745=
ENST00000620466.4:n.2038A>T
NM_015120.4:c.8238A>T , LRG_741t1:c.8238A>T	NP_055935.4:p.Ala2746=
NM_001378454.1:c.8235A>T MANE Select	NP_001365383.1:p.Ala2745=