Canonical Allele Identifier: CA50391571

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73448930T>C , CM000664.2:g.73448930T>C	GRCh38
NC_000002.11:g.73676057T>C , CM000664.1:g.73676057T>C	GRCh37
NC_000002.10:g.73529565T>C	NCBI36
NG_011690.1:g.68178T>C , LRG_741:g.68178T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.2403T>C MANE Select	NP_001365383.1:p.Thr801=
ENST00000613296.6:c.2403T>C MANE Select	ENSP00000482968.1:p.Thr801=
NM_015120.4:c.2406T>C , LRG_741t1:c.2406T>C	NP_055935.4:p.Thr802=
ENST00000484298.5:c.2277T>C	ENSP00000478155.1:p.Thr759=
ENST00000613296.4:c.2403T>C	ENSP00000482968.1:p.Thr801=
ENST00000614410.4:c.2403T>C	ENSP00000479094.1:p.Thr801=
ENST00000682565.1:c.2022T>C	ENSP00000507671.1:p.Thr674=
ENST00000682801.1:c.2022T>C	ENSP00000507862.1:p.Thr674=
ENST00000682859.1:c.2022T>C	ENSP00000508222.1:p.Thr674=
ENST00000683791.1:c.685+16639T>C
ENST00000684548.1:c.2022T>C	ENSP00000507421.1:p.Thr674=