Canonical Allele Identifier: CA347268420

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717439G>C (hg19) ; chr2:g.73490312G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490312G>C , CM000664.2:g.73490312G>C	GRCh38
NC_000002.11:g.73717439G>C , CM000664.1:g.73717439G>C	GRCh37
NC_000002.10:g.73570947G>C	NCBI36
NG_011690.1:g.109560G>C , LRG_741:g.109560G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7972G>C	ENSP00000507671.1:p.Val2658Leu
ENST00000682801.1:c.7972G>C	ENSP00000507862.1:p.Val2658Leu
ENST00000682859.1:c.7972G>C	ENSP00000508222.1:p.Val2658Leu
ENST00000683791.1:c.1364G>C
ENST00000684460.1:c.5424G>C
ENST00000684548.1:c.7972G>C	ENSP00000507421.1:p.Val2658Leu
ENST00000684590.1:c.2419G>C	ENSP00000507376.1:p.Val807Leu
ENST00000684656.1:c.5424G>C
ENST00000613296.6:c.8353G>C MANE Select	ENSP00000482968.1:p.Val2785Leu
ENST00000651434.1:c.896-29463G>C
ENST00000423048.5:c.3030+154G>C	ENSP00000399833.1:n.3030+154G>C
ENST00000484298.5:c.8227G>C	ENSP00000478155.1:p.Val2743Leu
ENST00000613296.4:c.8353G>C	ENSP00000482968.1:p.Val2785Leu
ENST00000614410.4:c.8353G>C	ENSP00000479094.1:p.Val2785Leu
ENST00000620466.4:n.2156G>C
NM_015120.4:c.8356G>C , LRG_741t1:c.8356G>C	NP_055935.4:p.Val2786Leu
NM_001378454.1:c.8353G>C MANE Select	NP_001365383.1:p.Val2785Leu