Canonical Allele Identifier: CA427024153

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799681G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572554G>C , CM000664.2:g.73572554G>C	GRCh38
NC_000002.11:g.73799681G>C , CM000664.1:g.73799681G>C	GRCh37
NC_000002.10:g.73653189G>C	NCBI36
NG_011690.1:g.191802G>C , LRG_741:g.191802G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10296G>C	ENSP00000507671.1:p.Val3432=
ENST00000682801.1:c.10296G>C	ENSP00000507862.1:p.Val3432=
ENST00000682859.1:c.10296G>C	ENSP00000508222.1:p.Val3432=
ENST00000683791.1:c.3382G>C
ENST00000684460.1:c.7577G>C
ENST00000684548.1:c.10296G>C	ENSP00000507421.1:p.Val3432=
ENST00000684590.1:c.4743G>C	ENSP00000507376.1:p.Val1581=
ENST00000684656.1:c.7622G>C
ENST00000613296.6:c.10677G>C MANE Select	ENSP00000482968.1:p.Val3559=
ENST00000651057.1:c.831G>C	ENSP00000498504.1:p.Val277=
ENST00000651434.1:c.2033G>C
ENST00000651750.1:c.65G>C
ENST00000652487.1:c.1774G>C
ENST00000423048.5:c.4168G>C	ENSP00000399833.1:n.4168G>C
ENST00000484298.5:c.10551G>C	ENSP00000478155.1:p.Val3517=
ENST00000613296.4:c.10677G>C	ENSP00000482968.1:p.Val3559=
ENST00000614410.4:c.10677G>C	ENSP00000479094.1:p.Val3559=
ENST00000620466.4:n.4480G>C
NM_015120.4:c.10680G>C , LRG_741t1:c.10680G>C	NP_055935.4:p.Val3560=
NM_001378454.1:c.10677G>C MANE Select	NP_001365383.1:p.Val3559=