Canonical Allele Identifier: CA427024430

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73800026G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572899G>A , CM000664.2:g.73572899G>A	GRCh38
NC_000002.11:g.73800026G>A , CM000664.1:g.73800026G>A	GRCh37
NC_000002.10:g.73653534G>A	NCBI36
NG_011690.1:g.192147G>A , LRG_741:g.192147G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10641G>A	ENSP00000507671.1:p.Gln3547=
ENST00000682801.1:c.10641G>A	ENSP00000507862.1:p.Gln3547=
ENST00000682859.1:c.10641G>A	ENSP00000508222.1:p.Gln3547=
ENST00000683791.1:c.3727G>A
ENST00000684460.1:c.7922G>A
ENST00000684548.1:c.10641G>A	ENSP00000507421.1:p.Gln3547=
ENST00000684590.1:c.5088G>A	ENSP00000507376.1:p.Gln1696=
ENST00000684656.1:c.7967G>A
ENST00000613296.6:c.11022G>A MANE Select	ENSP00000482968.1:p.Gln3674=
ENST00000651057.1:c.1176G>A	ENSP00000498504.1:p.Gln392=
ENST00000651434.1:c.2378G>A
ENST00000651750.1:c.410G>A
ENST00000652487.1:c.2119G>A
ENST00000423048.5:c.4513G>A	ENSP00000399833.1:n.4513G>A
ENST00000484298.5:c.10896G>A	ENSP00000478155.1:p.Gln3632=
ENST00000613296.4:c.11022G>A	ENSP00000482968.1:p.Gln3674=
ENST00000614410.4:c.11022G>A	ENSP00000479094.1:p.Gln3674=
ENST00000620466.4:n.4825G>A
NM_015120.4:c.11025G>A , LRG_741t1:c.11025G>A	NP_055935.4:p.Gln3675=
NM_001378454.1:c.11022G>A MANE Select	NP_001365383.1:p.Gln3674=