Canonical Allele Identifier: CA375369842

Gene: TSC1

Linked Data

• ClinVar Variation Id: 2806132
• ClinVar RCV Id: RCV003613556
• MyVariant Identifiers: chr9:g.135776109G>A (hg19) ; chr9:g.132900722G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132900722G>A , CM000671.2:g.132900722G>A	GRCh38
NC_000009.11:g.135776109G>A , CM000671.1:g.135776109G>A	GRCh37
NC_000009.10:g.134765930G>A	NCBI36
NG_012386.1:g.48912C>T , LRG_486:g.48912C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.2615C>T	ENSP00000496126.2:p.Thr872Ile
ENST00000490179.4:c.2618C>T	ENSP00000495533.2:p.Thr873Ile
ENST00000642261.2:c.*397C>T	ENSP00000494743.2:n.*397C>T
ENST00000643275.2:c.*558C>T	ENSP00000495598.2:n.*558C>T
ENST00000643362.2:c.2231C>T	ENSP00000496398.2:p.Thr744Ile
ENST00000643625.2:c.*360C>T	ENSP00000495546.2:n.*360C>T
ENST00000643691.2:c.2255C>T	ENSP00000494916.2:p.Thr752Ile
ENST00000644184.2:c.2576C>T	ENSP00000495428.2:p.Thr859Ile
ENST00000645129.2:c.2462C>T	ENSP00000493639.2:p.Thr821Ile
ENST00000646440.2:c.2618C>T	ENSP00000495830.2:p.Thr873Ile
ENST00000298552.9:c.2618C>T MANE Select	ENSP00000298552.3:p.Thr873Ile
ENST00000642261.1:c.678C>T
ENST00000642617.1:c.2615C>T	ENSP00000493773.1:p.Thr872Ile
ENST00000642627.1:c.2600C>T	ENSP00000496772.1:p.Thr867Ile
ENST00000642811.1:c.*2388C>T	ENSP00000495554.1:n.*2388C>T
ENST00000643072.1:c.2465C>T	ENSP00000496691.1:p.Thr822Ile
ENST00000643275.1:c.1092C>T	ENSP00000495598.1:n.1092C>T
ENST00000643583.1:c.2603C>T	ENSP00000494685.1:p.Thr868Ile
ENST00000643625.1:c.495C>T	ENSP00000495546.1:n.495C>T
ENST00000643875.1:c.2618C>T	ENSP00000495158.1:p.Thr873Ile
ENST00000644097.1:c.2615C>T	ENSP00000494682.1:p.Thr872Ile
ENST00000644184.1:c.1313C>T	ENSP00000495428.1:p.Thr438Ile
ENST00000644255.1:c.*2385C>T	ENSP00000493608.1:n.*2385C>T
ENST00000644319.1:n.2993C>T
ENST00000644786.1:n.277C>T
ENST00000644882.1:n.1531C>T
ENST00000645901.1:n.3469C>T
ENST00000646391.1:c.*2388C>T	ENSP00000494104.1:n.*2388C>T
ENST00000646625.1:c.2618C>T	ENSP00000496263.1:p.Thr873Ile
ENST00000647262.1:n.1583C>T
ENST00000647279.1:c.*1857C>T	ENSP00000494502.1:n.*1857C>T
ENST00000647506.1:n.3494C>T
ENST00000647534.1:n.1682C>T
ENST00000298552.7:c.2618C>T	ENSP00000298552.3:p.Thr873Ile
ENST00000440111.6:c.2618C>T	ENSP00000394524.2:p.Thr873Ile
ENST00000545250.5:c.2465C>T	ENSP00000444017.1:p.Thr822Ile
NM_000368.4:c.2618C>T , LRG_486t1:c.2618C>T	NP_000359.1:p.Thr873Ile
NM_001162426.1:c.2615C>T	NP_001155898.1:p.Thr872Ile
NM_001162427.1:c.2465C>T	NP_001155899.1:p.Thr822Ile
XM_005272211.1:c.2618C>T	XP_005272268.1:p.Thr873Ile
XM_006717271.1:c.2618C>T	XP_006717334.1:p.Thr873Ile
XM_011518979.1:c.2618C>T	XP_011517281.1:p.Thr873Ile
NM_001362177.1:c.2255C>T	NP_001349106.1:p.Thr752Ile
XM_011518979.2:c.2618C>T	XP_011517281.1:p.Thr873Ile
XM_017015096.1:c.2618C>T	XP_016870585.1:p.Thr873Ile
XM_017015097.1:c.2618C>T	XP_016870586.1:p.Thr873Ile
XM_017015098.1:c.2615C>T	XP_016870587.1:p.Thr872Ile
XM_017015100.1:c.2255C>T	XP_016870589.1:p.Thr752Ile
XM_017015101.1:c.2252C>T	XP_016870590.1:p.Thr751Ile
NM_000368.5:c.2618C>T MANE Select	NP_000359.1:p.Thr873Ile
NM_001162426.2:c.2615C>T	NP_001155898.1:p.Thr872Ile
NM_001162427.2:c.2465C>T	NP_001155899.1:p.Thr822Ile
NM_001362177.2:c.2255C>T	NP_001349106.1:p.Thr752Ile