Canonical Allele Identifier: CA2692285440

Gene: TSC1

Linked Data

• gnomAD v4: 9-132895879-GTTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132895880_132895882del , CM000671.2:g.132895880_132895882del	GRCh38
NC_000009.11:g.135771267_135771269del , CM000671.1:g.135771267_135771269del	GRCh37
NC_000009.10:g.134761088_134761090del	NCBI36
NG_012386.1:g.53752_53754del , LRG_486:g.53752_53754del

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.*353_*355del	ENSP00000496126.2:n.*353_*355del
ENST00000490179.4:c.*353_*355del	ENSP00000495533.2:n.*353_*355del
ENST00000642261.2:c.*1704_*1706del	ENSP00000494743.2:n.*1704_*1706del
ENST00000643275.2:c.*1788_*1790del	ENSP00000495598.2:n.*1788_*1790del
ENST00000643362.2:c.*353_*355del	ENSP00000496398.2:n.*353_*355del
ENST00000643625.2:c.*1590_*1592del	ENSP00000495546.2:n.*1590_*1592del
ENST00000643691.2:c.*353_*355del	ENSP00000494916.2:n.*353_*355del
ENST00000644184.2:c.*353_*355del	ENSP00000495428.2:n.*353_*355del
ENST00000645129.2:c.*353_*355del	ENSP00000493639.2:n.*353_*355del
ENST00000646440.2:c.*353_*355del	ENSP00000495830.2:n.*353_*355del
ENST00000298552.9:c.*353_*355del MANE Select	ENSP00000298552.3:n.*353_*355del
ENST00000642627.1:c.*353_*355del	ENSP00000496772.1:n.*353_*355del
ENST00000642811.1:c.*3618_*3620del	ENSP00000495554.1:n.*3618_*3620del
ENST00000643625.1:c.1725_1727del	ENSP00000495546.1:n.1725_1727del
ENST00000643875.1:c.*353_*355del	ENSP00000495158.1:n.*353_*355del
ENST00000644097.1:c.*353_*355del	ENSP00000494682.1:n.*353_*355del
ENST00000644184.1:c.2543_2545del	ENSP00000495428.1:n.2543_2545del
ENST00000644786.1:n.1507_1509del
ENST00000644882.1:n.2756_2758del
ENST00000645901.1:n.4699_4701del
ENST00000646625.1:c.*353_*355del	ENSP00000496263.1:n.*353_*355del
ENST00000647262.1:n.2813_2815del
ENST00000647534.1:n.2912_2914del
ENST00000298552.7:c.*353_*355del	ENSP00000298552.3:n.*353_*355del
ENST00000440111.6:c.*353_*355del	ENSP00000394524.2:n.*353_*355del
ENST00000545250.5:c.*353_*355del	ENSP00000444017.1:n.*353_*355del
NM_000368.4:c.*353_*355del , LRG_486t1:c.*353_*355del	NP_000359.1:n.*353_*355del
NM_001162426.1:c.*353_*355del	NP_001155898.1:n.*353_*355del
NM_001162427.1:c.*353_*355del	NP_001155899.1:n.*353_*355del
XM_005272211.1:c.*353_*355del	XP_005272268.1:n.*353_*355del
XM_006717271.1:c.*353_*355del	XP_006717334.1:n.*353_*355del
XM_011518979.1:c.*353_*355del	XP_011517281.1:n.*353_*355del
NM_001362177.1:c.*353_*355del	NP_001349106.1:n.*353_*355del
XM_011518979.2:c.*353_*355del	XP_011517281.1:n.*353_*355del
XM_017015096.1:c.*353_*355del	XP_016870585.1:n.*353_*355del
XM_017015097.1:c.*353_*355del	XP_016870586.1:n.*353_*355del
XM_017015098.1:c.*353_*355del	XP_016870587.1:n.*353_*355del
XM_017015100.1:c.*353_*355del	XP_016870589.1:n.*353_*355del
XM_017015101.1:c.*353_*355del	XP_016870590.1:n.*353_*355del
NM_000368.5:c.*353_*355del MANE Select	NP_000359.1:n.*353_*355del
NM_001162426.2:c.*353_*355del	NP_001155898.1:n.*353_*355del
NM_001162427.2:c.*353_*355del	NP_001155899.1:n.*353_*355del
NM_001362177.2:c.*353_*355del	NP_001349106.1:n.*353_*355del