Canonical Allele Identifier: CA347269419

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490522G>T , CM000664.2:g.73490522G>T	GRCh38
NC_000002.11:g.73717649G>T , CM000664.1:g.73717649G>T	GRCh37
NC_000002.10:g.73571157G>T	NCBI36
NG_011690.1:g.109770G>T , LRG_741:g.109770G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.8563G>T MANE Select	NP_001365383.1:p.Gly2855Ter
ENST00000613296.6:c.8563G>T MANE Select	ENSP00000482968.1:p.Gly2855Ter
NM_015120.4:c.8566G>T , LRG_741t1:c.8566G>T	NP_055935.4:p.Gly2856Ter
ENST00000423048.5:c.3030+364G>T	ENSP00000399833.1:n.3030+364G>T
ENST00000484298.5:c.8437G>T	ENSP00000478155.1:p.Gly2813Ter
ENST00000613296.4:c.8563G>T	ENSP00000482968.1:p.Gly2855Ter
ENST00000614410.4:c.8563G>T	ENSP00000479094.1:p.Gly2855Ter
ENST00000620466.4:n.2366G>T
ENST00000651434.1:c.896-29253G>T
ENST00000682565.1:c.8182G>T	ENSP00000507671.1:p.Gly2728Ter
ENST00000682801.1:c.8182G>T	ENSP00000507862.1:p.Gly2728Ter
ENST00000682859.1:c.8182G>T	ENSP00000508222.1:p.Gly2728Ter
ENST00000683791.1:c.1574G>T
ENST00000684460.1:c.5634G>T
ENST00000684548.1:c.8182G>T	ENSP00000507421.1:p.Gly2728Ter
ENST00000684590.1:c.2629G>T	ENSP00000507376.1:p.Gly877Ter
ENST00000684656.1:c.5634G>T