Canonical Allele Identifier: CA347263935

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716812C>T (hg19) ; chr2:g.73489685C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489685C>T , CM000664.2:g.73489685C>T	GRCh38
NC_000002.11:g.73716812C>T , CM000664.1:g.73716812C>T	GRCh37
NC_000002.10:g.73570320C>T	NCBI36
NG_011690.1:g.108933C>T , LRG_741:g.108933C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7345C>T	ENSP00000507671.1:p.His2449Tyr
ENST00000682801.1:c.7345C>T	ENSP00000507862.1:p.His2449Tyr
ENST00000682859.1:c.7345C>T	ENSP00000508222.1:p.His2449Tyr
ENST00000683791.1:c.737C>T
ENST00000684460.1:c.4797C>T
ENST00000684548.1:c.7345C>T	ENSP00000507421.1:p.His2449Tyr
ENST00000684590.1:c.1792C>T	ENSP00000507376.1:p.His598Tyr
ENST00000684656.1:c.4797C>T
ENST00000613296.6:c.7726C>T MANE Select	ENSP00000482968.1:p.His2576Tyr
ENST00000651434.1:c.896-30090C>T
ENST00000423048.5:c.2557C>T	ENSP00000399833.1:p.His853Tyr
ENST00000484298.5:c.7600C>T	ENSP00000478155.1:p.His2534Tyr
ENST00000613296.4:c.7726C>T	ENSP00000482968.1:p.His2576Tyr
ENST00000614410.4:c.7726C>T	ENSP00000479094.1:p.His2576Tyr
ENST00000620466.4:n.1529C>T
NM_015120.4:c.7729C>T , LRG_741t1:c.7729C>T	NP_055935.4:p.His2577Tyr
NM_001378454.1:c.7726C>T MANE Select	NP_001365383.1:p.His2576Tyr