Canonical Allele Identifier: CA427023372

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73453347C>T , CM000664.2:g.73453347C>T	GRCh38
NC_000002.11:g.73680474C>T , CM000664.1:g.73680474C>T	GRCh37
NC_000002.10:g.73533982C>T	NCBI36
NG_011690.1:g.72595C>T , LRG_741:g.72595C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.6820C>T MANE Select	NP_001365383.1:p.Leu2274=
ENST00000613296.6:c.6820C>T MANE Select	ENSP00000482968.1:p.Leu2274=
NM_015120.4:c.6823C>T , LRG_741t1:c.6823C>T	NP_055935.4:p.Leu2275=
ENST00000423048.5:c.1651C>T	ENSP00000399833.1:p.Leu551=
ENST00000484298.5:c.6694C>T	ENSP00000478155.1:p.Leu2232=
ENST00000613296.4:c.6820C>T	ENSP00000482968.1:p.Leu2274=
ENST00000614410.4:c.6820C>T	ENSP00000479094.1:p.Leu2274=
ENST00000620466.4:n.623C>T
ENST00000651434.1:c.41C>T
ENST00000682565.1:c.6439C>T	ENSP00000507671.1:p.Leu2147=
ENST00000682801.1:c.6439C>T	ENSP00000507862.1:p.Leu2147=
ENST00000682859.1:c.6439C>T	ENSP00000508222.1:p.Leu2147=
ENST00000683791.1:c.685+21056C>T
ENST00000684197.1:n.1789C>T
ENST00000684460.1:c.3891C>T
ENST00000684548.1:c.6439C>T	ENSP00000507421.1:p.Leu2147=
ENST00000684590.1:c.937C>T	ENSP00000507376.1:p.Leu313=
ENST00000684656.1:c.3891C>T