Canonical Allele Identifier: CA1714149

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73453453C>T , CM000664.2:g.73453453C>T	GRCh38
NC_000002.11:g.73680580C>T , CM000664.1:g.73680580C>T	GRCh37
NC_000002.10:g.73534088C>T	NCBI36
NG_011690.1:g.72701C>T , LRG_741:g.72701C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.6926C>T MANE Select	NP_001365383.1:p.Thr2309Met
ENST00000613296.6:c.6926C>T MANE Select	ENSP00000482968.1:p.Thr2309Met
NM_015120.4:c.6929C>T , LRG_741t1:c.6929C>T	NP_055935.4:p.Thr2310Met
ENST00000423048.5:c.1757C>T	ENSP00000399833.1:p.Thr586Met
ENST00000484298.5:c.6800C>T	ENSP00000478155.1:p.Thr2267Met
ENST00000613296.4:c.6926C>T	ENSP00000482968.1:p.Thr2309Met
ENST00000614410.4:c.6926C>T	ENSP00000479094.1:p.Thr2309Met
ENST00000620466.4:n.729C>T
ENST00000651434.1:c.147C>T
ENST00000682565.1:c.6545C>T	ENSP00000507671.1:p.Thr2182Met
ENST00000682801.1:c.6545C>T	ENSP00000507862.1:p.Thr2182Met
ENST00000682859.1:c.6545C>T	ENSP00000508222.1:p.Thr2182Met
ENST00000683791.1:c.685+21162C>T
ENST00000684197.1:n.1895C>T
ENST00000684460.1:c.3997C>T
ENST00000684548.1:c.6545C>T	ENSP00000507421.1:p.Thr2182Met
ENST00000684590.1:c.1043C>T	ENSP00000507376.1:p.Thr348Met
ENST00000684656.1:c.3997C>T