Canonical Allele Identifier: CA1713960

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73452445C>A , CM000664.2:g.73452445C>A	GRCh38
NC_000002.11:g.73679572C>A , CM000664.1:g.73679572C>A	GRCh37
NC_000002.10:g.73533080C>A	NCBI36
NG_011690.1:g.71693C>A , LRG_741:g.71693C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.5918C>A MANE Select	NP_001365383.1:p.Pro1973Gln
ENST00000613296.6:c.5918C>A MANE Select	ENSP00000482968.1:p.Pro1973Gln
NM_015120.4:c.5921C>A , LRG_741t1:c.5921C>A	NP_055935.4:p.Pro1974Gln
ENST00000423048.5:c.749C>A	ENSP00000399833.1:p.Pro250Gln
ENST00000484298.5:c.5792C>A	ENSP00000478155.1:p.Pro1931Gln
ENST00000613296.4:c.5918C>A	ENSP00000482968.1:p.Pro1973Gln
ENST00000614410.4:c.5918C>A	ENSP00000479094.1:p.Pro1973Gln
ENST00000682565.1:c.5537C>A	ENSP00000507671.1:p.Pro1846Gln
ENST00000682801.1:c.5537C>A	ENSP00000507862.1:p.Pro1846Gln
ENST00000682859.1:c.5537C>A	ENSP00000508222.1:p.Pro1846Gln
ENST00000683791.1:c.685+20154C>A
ENST00000684197.1:n.887C>A
ENST00000684460.1:c.2989C>A
ENST00000684548.1:c.5537C>A	ENSP00000507421.1:p.Pro1846Gln
ENST00000684590.1:c.35C>A	ENSP00000507376.1:p.Pro12Gln
ENST00000684656.1:c.2989C>A