Canonical Allele Identifier: CA2609362367

Gene: SIRT1

Linked Data

• gnomAD v4: 10-67916991-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916993_67916994del , CM000672.2:g.67916993_67916994del	GRCh38
NC_000010.10:g.69676750_69676751del , CM000672.1:g.69676750_69676751del	GRCh37
NC_000010.9:g.69346756_69346757del	NCBI36
NG_050664.1:g.37332_37333del

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*400_*401del MANE Select	ENSP00000212015.6:n.*400_*401del
ENST00000212015.10:c.*400_*401del	ENSP00000212015.6:n.*400_*401del
ENST00000403579.1:c.*400_*401del	ENSP00000384063.1:n.*400_*401del
ENST00000406900.5:c.*400_*401del	ENSP00000384508.1:n.*400_*401del
ENST00000432464.5:c.*400_*401del	ENSP00000409208.1:n.*400_*401del
NM_001142498.1:c.*400_*401del	NP_001135970.1:n.*400_*401del
NM_001314049.1:c.*400_*401del	NP_001300978.1:n.*400_*401del
NM_012238.4:c.*400_*401del	NP_036370.2:n.*400_*401del
XM_006717737.2:c.*400_*401del	XP_006717800.1:n.*400_*401del
XM_011539561.1:c.*400_*401del	XP_011537863.1:n.*400_*401del
NM_012238.5:c.*400_*401del MANE Select	NP_036370.2:n.*400_*401del
NM_001142498.2:c.*400_*401del	NP_001135970.1:n.*400_*401del