Canonical Allele Identifier: CA347285156

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799737G>C (hg19) ; chr2:g.73572610G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572610G>C , CM000664.2:g.73572610G>C	GRCh38
NC_000002.11:g.73799737G>C , CM000664.1:g.73799737G>C	GRCh37
NC_000002.10:g.73653245G>C	NCBI36
NG_011690.1:g.191858G>C , LRG_741:g.191858G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10352G>C	ENSP00000507671.1:p.Ser3451Thr
ENST00000682801.1:c.10352G>C	ENSP00000507862.1:p.Ser3451Thr
ENST00000682859.1:c.10352G>C	ENSP00000508222.1:p.Ser3451Thr
ENST00000683791.1:c.3438G>C
ENST00000684460.1:c.7633G>C
ENST00000684548.1:c.10352G>C	ENSP00000507421.1:p.Ser3451Thr
ENST00000684590.1:c.4799G>C	ENSP00000507376.1:p.Ser1600Thr
ENST00000684656.1:c.7678G>C
ENST00000613296.6:c.10733G>C MANE Select	ENSP00000482968.1:p.Ser3578Thr
ENST00000651057.1:c.887G>C	ENSP00000498504.1:p.Ser296Thr
ENST00000651434.1:c.2089G>C
ENST00000651750.1:c.121G>C
ENST00000652487.1:c.1830G>C
ENST00000423048.5:c.4224G>C	ENSP00000399833.1:n.4224G>C
ENST00000484298.5:c.10607G>C	ENSP00000478155.1:p.Ser3536Thr
ENST00000613296.4:c.10733G>C	ENSP00000482968.1:p.Ser3578Thr
ENST00000614410.4:c.10733G>C	ENSP00000479094.1:p.Ser3578Thr
ENST00000620466.4:n.4536G>C
NM_015120.4:c.10736G>C , LRG_741t1:c.10736G>C	NP_055935.4:p.Ser3579Thr
NM_001378454.1:c.10733G>C MANE Select	NP_001365383.1:p.Ser3578Thr