Canonical Allele Identifier: CA347267199

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828551A>C (hg19) ; chr2:g.73601424A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601424A>C , CM000664.2:g.73601424A>C	GRCh38
NC_000002.11:g.73828551A>C , CM000664.1:g.73828551A>C	GRCh37
NC_000002.10:g.73682059A>C	NCBI36
NG_011690.1:g.220672A>C , LRG_741:g.220672A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11721A>C	ENSP00000507671.1:p.Arg3907Ser
ENST00000682801.1:c.11167-761A>C	ENSP00000507862.1:n.11167-761A>C
ENST00000682859.1:c.11721A>C	ENSP00000508222.1:p.Arg3907Ser
ENST00000683791.1:c.4807A>C
ENST00000684460.1:c.9002A>C
ENST00000684548.1:c.11721A>C	ENSP00000507421.1:p.Arg3907Ser
ENST00000684590.1:c.6168A>C	ENSP00000507376.1:p.Arg2056Ser
ENST00000684656.1:c.9186A>C
ENST00000613296.6:c.12102A>C MANE Select	ENSP00000482968.1:p.Arg4034Ser
ENST00000651057.1:c.2256A>C	ENSP00000498504.1:p.Arg752Ser
ENST00000651434.1:c.3458A>C
ENST00000651750.1:c.1260+543A>C
ENST00000652487.1:c.3273A>C
ENST00000464408.3:n.277A>C
ENST00000484298.5:c.11976A>C	ENSP00000478155.1:p.Arg3992Ser
ENST00000613296.4:c.12102A>C	ENSP00000482968.1:p.Arg4034Ser
ENST00000620466.4:n.5905A>C
NM_015120.4:c.12105A>C , LRG_741t1:c.12105A>C	NP_055935.4:p.Arg4035Ser
NM_001378454.1:c.12102A>C MANE Select	NP_001365383.1:p.Arg4034Ser