Canonical Allele Identifier: CA347286814

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73800009C>A (hg19) ; chr2:g.73572882C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572882C>A , CM000664.2:g.73572882C>A	GRCh38
NC_000002.11:g.73800009C>A , CM000664.1:g.73800009C>A	GRCh37
NC_000002.10:g.73653517C>A	NCBI36
NG_011690.1:g.192130C>A , LRG_741:g.192130C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10624C>A	ENSP00000507671.1:p.Gln3542Lys
ENST00000682801.1:c.10624C>A	ENSP00000507862.1:p.Gln3542Lys
ENST00000682859.1:c.10624C>A	ENSP00000508222.1:p.Gln3542Lys
ENST00000683791.1:c.3710C>A
ENST00000684460.1:c.7905C>A
ENST00000684548.1:c.10624C>A	ENSP00000507421.1:p.Gln3542Lys
ENST00000684590.1:c.5071C>A	ENSP00000507376.1:p.Gln1691Lys
ENST00000684656.1:c.7950C>A
ENST00000613296.6:c.11005C>A MANE Select	ENSP00000482968.1:p.Gln3669Lys
ENST00000651057.1:c.1159C>A	ENSP00000498504.1:p.Gln387Lys
ENST00000651434.1:c.2361C>A
ENST00000651750.1:c.393C>A
ENST00000652487.1:c.2102C>A
ENST00000423048.5:c.4496C>A	ENSP00000399833.1:n.4496C>A
ENST00000484298.5:c.10879C>A	ENSP00000478155.1:p.Gln3627Lys
ENST00000613296.4:c.11005C>A	ENSP00000482968.1:p.Gln3669Lys
ENST00000614410.4:c.11005C>A	ENSP00000479094.1:p.Gln3669Lys
ENST00000620466.4:n.4808C>A
NM_015120.4:c.11008C>A , LRG_741t1:c.11008C>A	NP_055935.4:p.Gln3670Lys
NM_001378454.1:c.11005C>A MANE Select	NP_001365383.1:p.Gln3669Lys