Canonical Allele Identifier: CA347284553

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799662A>C (hg19) ; chr2:g.73572535A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572535A>C , CM000664.2:g.73572535A>C	GRCh38
NC_000002.11:g.73799662A>C , CM000664.1:g.73799662A>C	GRCh37
NC_000002.10:g.73653170A>C	NCBI36
NG_011690.1:g.191783A>C , LRG_741:g.191783A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10277A>C	ENSP00000507671.1:p.Asn3426Thr
ENST00000682801.1:c.10277A>C	ENSP00000507862.1:p.Asn3426Thr
ENST00000682859.1:c.10277A>C	ENSP00000508222.1:p.Asn3426Thr
ENST00000683791.1:c.3363A>C
ENST00000684460.1:c.7558A>C
ENST00000684548.1:c.10277A>C	ENSP00000507421.1:p.Asn3426Thr
ENST00000684590.1:c.4724A>C	ENSP00000507376.1:p.Asn1575Thr
ENST00000684656.1:c.7603A>C
ENST00000613296.6:c.10658A>C MANE Select	ENSP00000482968.1:p.Asn3553Thr
ENST00000651057.1:c.812A>C	ENSP00000498504.1:p.Asn271Thr
ENST00000651434.1:c.2014A>C
ENST00000651750.1:c.46A>C
ENST00000652487.1:c.1755A>C
ENST00000423048.5:c.4149A>C	ENSP00000399833.1:n.4149A>C
ENST00000484298.5:c.10532A>C	ENSP00000478155.1:p.Asn3511Thr
ENST00000613296.4:c.10658A>C	ENSP00000482968.1:p.Asn3553Thr
ENST00000614410.4:c.10658A>C	ENSP00000479094.1:p.Asn3553Thr
ENST00000620466.4:n.4461A>C
NM_015120.4:c.10661A>C , LRG_741t1:c.10661A>C	NP_055935.4:p.Asn3554Thr
NM_001378454.1:c.10658A>C MANE Select	NP_001365383.1:p.Asn3553Thr