Canonical Allele Identifier: CA1713885

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73451979C>T , CM000664.2:g.73451979C>T	GRCh38
NC_000002.11:g.73679106C>T , CM000664.1:g.73679106C>T	GRCh37
NC_000002.10:g.73532614C>T	NCBI36
NG_011690.1:g.71227C>T , LRG_741:g.71227C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.5452C>T MANE Select	NP_001365383.1:p.Arg1818Ter
ENST00000613296.6:c.5452C>T MANE Select	ENSP00000482968.1:p.Arg1818Ter
NM_015120.4:c.5455C>T , LRG_741t1:c.5455C>T	NP_055935.4:p.Arg1819Ter
ENST00000423048.5:c.283C>T	ENSP00000399833.1:p.Arg95Ter
ENST00000484298.5:c.5326C>T	ENSP00000478155.1:p.Arg1776Ter
ENST00000613296.4:c.5452C>T	ENSP00000482968.1:p.Arg1818Ter
ENST00000614410.4:c.5452C>T	ENSP00000479094.1:p.Arg1818Ter
ENST00000682565.1:c.5071C>T	ENSP00000507671.1:p.Arg1691Ter
ENST00000682801.1:c.5071C>T	ENSP00000507862.1:p.Arg1691Ter
ENST00000682859.1:c.5071C>T	ENSP00000508222.1:p.Arg1691Ter
ENST00000683791.1:c.685+19688C>T
ENST00000684197.1:n.421C>T
ENST00000684460.1:c.2523C>T
ENST00000684548.1:c.5071C>T	ENSP00000507421.1:p.Arg1691Ter
ENST00000684656.1:c.2523C>T