Canonical Allele Identifier: CA426765391

Gene: ALMS1

Linked Data

• dbSNP Id: rs1382859597
• gnomAD v2: 2-73716823-T-C
• gnomAD v4: 2-73489696-T-C
• MyVariant Identifiers: chr2:g.73716823T>C (hg19) ; chr2:g.73489696T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489696T>C , CM000664.2:g.73489696T>C	GRCh38
NC_000002.11:g.73716823T>C , CM000664.1:g.73716823T>C	GRCh37
NC_000002.10:g.73570331T>C	NCBI36
NG_011690.1:g.108944T>C , LRG_741:g.108944T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7356T>C	ENSP00000507671.1:p.Ile2452=
ENST00000682801.1:c.7356T>C	ENSP00000507862.1:p.Ile2452=
ENST00000682859.1:c.7356T>C	ENSP00000508222.1:p.Ile2452=
ENST00000683791.1:c.748T>C
ENST00000684460.1:c.4808T>C
ENST00000684548.1:c.7356T>C	ENSP00000507421.1:p.Ile2452=
ENST00000684590.1:c.1803T>C	ENSP00000507376.1:p.Ile601=
ENST00000684656.1:c.4808T>C
ENST00000613296.6:c.7737T>C MANE Select	ENSP00000482968.1:p.Ile2579=
ENST00000651434.1:c.896-30079T>C
ENST00000423048.5:c.2568T>C	ENSP00000399833.1:p.Ile856=
ENST00000484298.5:c.7611T>C	ENSP00000478155.1:p.Ile2537=
ENST00000613296.4:c.7737T>C	ENSP00000482968.1:p.Ile2579=
ENST00000614410.4:c.7737T>C	ENSP00000479094.1:p.Ile2579=
ENST00000620466.4:n.1540T>C
NM_015120.4:c.7740T>C , LRG_741t1:c.7740T>C	NP_055935.4:p.Ile2580=
NM_001378454.1:c.7737T>C MANE Select	NP_001365383.1:p.Ile2579=