Canonical Allele Identifier: CA427024216

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799717A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572590A>T , CM000664.2:g.73572590A>T	GRCh38
NC_000002.11:g.73799717A>T , CM000664.1:g.73799717A>T	GRCh37
NC_000002.10:g.73653225A>T	NCBI36
NG_011690.1:g.191838A>T , LRG_741:g.191838A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10332A>T	ENSP00000507671.1:p.Pro3444=
ENST00000682801.1:c.10332A>T	ENSP00000507862.1:p.Pro3444=
ENST00000682859.1:c.10332A>T	ENSP00000508222.1:p.Pro3444=
ENST00000683791.1:c.3418A>T
ENST00000684460.1:c.7613A>T
ENST00000684548.1:c.10332A>T	ENSP00000507421.1:p.Pro3444=
ENST00000684590.1:c.4779A>T	ENSP00000507376.1:p.Pro1593=
ENST00000684656.1:c.7658A>T
ENST00000613296.6:c.10713A>T MANE Select	ENSP00000482968.1:p.Pro3571=
ENST00000651057.1:c.867A>T	ENSP00000498504.1:p.Pro289=
ENST00000651434.1:c.2069A>T
ENST00000651750.1:c.101A>T
ENST00000652487.1:c.1810A>T
ENST00000423048.5:c.4204A>T	ENSP00000399833.1:n.4204A>T
ENST00000484298.5:c.10587A>T	ENSP00000478155.1:p.Pro3529=
ENST00000613296.4:c.10713A>T	ENSP00000482968.1:p.Pro3571=
ENST00000614410.4:c.10713A>T	ENSP00000479094.1:p.Pro3571=
ENST00000620466.4:n.4516A>T
NM_015120.4:c.10716A>T , LRG_741t1:c.10716A>T	NP_055935.4:p.Pro3572=
NM_001378454.1:c.10713A>T MANE Select	NP_001365383.1:p.Pro3571=