Canonical Allele Identifier: CA375367041

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132896530A>G , CM000671.2:g.132896530A>G	GRCh38
NC_000009.11:g.135771917A>G , CM000671.1:g.135771917A>G	GRCh37
NC_000009.10:g.134761738A>G	NCBI36
NG_012386.1:g.53104T>C , LRG_486:g.53104T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000368.5:c.3200T>C MANE Select	NP_000359.1:p.Met1067Thr
ENST00000298552.9:c.3200T>C MANE Select	ENSP00000298552.3:p.Met1067Thr
NM_000368.4:c.3200T>C , LRG_486t1:c.3200T>C	NP_000359.1:p.Met1067Thr
NM_001162426.1:c.3197T>C	NP_001155898.1:p.Met1066Thr
NM_001162426.2:c.3197T>C	NP_001155898.1:p.Met1066Thr
NM_001162427.1:c.3047T>C	NP_001155899.1:p.Met1016Thr
NM_001162427.2:c.3047T>C	NP_001155899.1:p.Met1016Thr
NM_001362177.1:c.2837T>C	NP_001349106.1:p.Met946Thr
NM_001362177.2:c.2837T>C	NP_001349106.1:p.Met946Thr
ENST00000298552.7:c.3200T>C	ENSP00000298552.3:p.Met1067Thr
ENST00000440111.6:c.3200T>C	ENSP00000394524.2:p.Met1067Thr
ENST00000475903.7:c.3197T>C	ENSP00000496126.2:p.Met1066Thr
ENST00000490179.4:c.3200T>C	ENSP00000495533.2:p.Met1067Thr
ENST00000545250.5:c.3047T>C	ENSP00000444017.1:p.Met1016Thr
ENST00000642261.2:c.*1056T>C	ENSP00000494743.2:n.*1056T>C
ENST00000642617.1:c.3197T>C	ENSP00000493773.1:p.Met1066Thr
ENST00000642627.1:c.3182T>C	ENSP00000496772.1:p.Met1061Thr
ENST00000642811.1:c.*2970T>C	ENSP00000495554.1:n.*2970T>C
ENST00000643072.1:c.3047T>C	ENSP00000496691.1:p.Met1016Thr
ENST00000643275.2:c.*1140T>C	ENSP00000495598.2:n.*1140T>C
ENST00000643362.2:c.2813T>C	ENSP00000496398.2:p.Met938Thr
ENST00000643583.1:c.3185T>C	ENSP00000494685.1:p.Met1062Thr
ENST00000643625.1:c.1077T>C	ENSP00000495546.1:n.1077T>C
ENST00000643625.2:c.*942T>C	ENSP00000495546.2:n.*942T>C
ENST00000643691.2:c.2837T>C	ENSP00000494916.2:p.Met946Thr
ENST00000643875.1:c.3200T>C	ENSP00000495158.1:p.Met1067Thr
ENST00000644097.1:c.3197T>C	ENSP00000494682.1:p.Met1066Thr
ENST00000644184.1:c.1895T>C	ENSP00000495428.1:p.Met632Thr
ENST00000644184.2:c.3158T>C	ENSP00000495428.2:p.Met1053Thr
ENST00000644255.1:c.*2967T>C	ENSP00000493608.1:n.*2967T>C
ENST00000644319.1:n.3575T>C
ENST00000644786.1:n.859T>C
ENST00000644882.1:n.2108T>C
ENST00000645129.2:c.3044T>C	ENSP00000493639.2:p.Met1015Thr
ENST00000645901.1:n.4051T>C
ENST00000646391.1:c.*2970T>C	ENSP00000494104.1:n.*2970T>C
ENST00000646440.2:c.3200T>C	ENSP00000495830.2:p.Met1067Thr
ENST00000646625.1:c.3200T>C	ENSP00000496263.1:p.Met1067Thr
ENST00000647262.1:n.2165T>C
ENST00000647279.1:c.*2439T>C	ENSP00000494502.1:n.*2439T>C
ENST00000647534.1:n.2264T>C
XM_005272211.1:c.3200T>C	XP_005272268.1:p.Met1067Thr
XM_006717271.1:c.3200T>C	XP_006717334.1:p.Met1067Thr
XM_011518979.1:c.3200T>C	XP_011517281.1:p.Met1067Thr
XM_011518979.2:c.3200T>C	XP_011517281.1:p.Met1067Thr
XM_017015096.1:c.3200T>C	XP_016870585.1:p.Met1067Thr
XM_017015097.1:c.3200T>C	XP_016870586.1:p.Met1067Thr
XM_017015098.1:c.3197T>C	XP_016870587.1:p.Met1066Thr
XM_017015100.1:c.2837T>C	XP_016870589.1:p.Met946Thr
XM_017015101.1:c.2834T>C	XP_016870590.1:p.Met945Thr