Canonical Allele Identifier: CA347284304

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799634A>T (hg19) ; chr2:g.73572507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572507A>T , CM000664.2:g.73572507A>T	GRCh38
NC_000002.11:g.73799634A>T , CM000664.1:g.73799634A>T	GRCh37
NC_000002.10:g.73653142A>T	NCBI36
NG_011690.1:g.191755A>T , LRG_741:g.191755A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682565.1:c.10249A>T	ENSP00000507671.1:p.Arg3417Ter
ENST00000682801.1:c.10249A>T	ENSP00000507862.1:p.Arg3417Ter
ENST00000682859.1:c.10249A>T	ENSP00000508222.1:p.Arg3417Ter
ENST00000683791.1:c.3335A>T
ENST00000684460.1:c.7530A>T
ENST00000684548.1:c.10249A>T	ENSP00000507421.1:p.Arg3417Ter
ENST00000684590.1:c.4696A>T	ENSP00000507376.1:p.Arg1566Ter
ENST00000684656.1:c.7575A>T
ENST00000613296.6:c.10630A>T MANE Select	ENSP00000482968.1:p.Arg3544Ter
ENST00000651057.1:c.784A>T	ENSP00000498504.1:p.Arg262Ter
ENST00000651434.1:c.1986A>T
ENST00000651750.1:c.18A>T
ENST00000652487.1:c.1727A>T
ENST00000423048.5:c.4121A>T	ENSP00000399833.1:n.4121A>T
ENST00000484298.5:c.10504A>T	ENSP00000478155.1:p.Arg3502Ter
ENST00000613296.4:c.10630A>T	ENSP00000482968.1:p.Arg3544Ter
ENST00000614410.4:c.10630A>T	ENSP00000479094.1:p.Arg3544Ter
ENST00000620466.4:n.4433A>T
NM_015120.4:c.10633A>T , LRG_741t1:c.10633A>T	NP_055935.4:p.Arg3545Ter
NM_001378454.1:c.10630A>T MANE Select	NP_001365383.1:p.Arg3544Ter