Canonical Allele Identifier: CA5763366

Gene: TUBGCP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133279775G>A , CM000672.2:g.133279775G>A	GRCh38
NC_000010.10:g.135093279G>A , CM000672.1:g.135093279G>A	GRCh37
NC_000010.9:g.134943269G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682093.1:c.*2205C>T	ENSP00000508354.1:n.*2205C>T
ENST00000682123.1:c.2700C>T	ENSP00000507610.1:p.Thr900=
ENST00000682161.1:c.2769C>T	ENSP00000507509.1:p.Thr923=
ENST00000682256.1:n.3927C>T
ENST00000682332.1:n.3136C>T
ENST00000682515.1:c.2700C>T	ENSP00000506731.1:p.Thr900=
ENST00000682591.1:n.1882C>T
ENST00000682631.1:c.*2728C>T	ENSP00000507220.1:n.*2728C>T
ENST00000682905.1:c.2733C>T	ENSP00000507305.1:p.Thr911=
ENST00000682990.1:c.*943C>T	ENSP00000506868.1:n.*943C>T
ENST00000683014.1:c.2667C>T	ENSP00000507631.1:p.Thr889=
ENST00000683060.1:c.2571C>T	ENSP00000508258.1:p.Thr857=
ENST00000683308.1:n.1813C>T
ENST00000683383.1:c.2580C>T	ENSP00000507601.1:p.Thr860=
ENST00000683612.1:c.2700C>T	ENSP00000507482.1:p.Thr900=
ENST00000683673.1:n.3217C>T
ENST00000683786.1:c.*2507C>T	ENSP00000508200.1:n.*2507C>T
ENST00000683829.1:c.*2679C>T	ENSP00000508146.1:n.*2679C>T
ENST00000684478.1:c.*2424C>T	ENSP00000507361.1:n.*2424C>T
ENST00000684487.1:c.*1016C>T	ENSP00000507802.1:n.*1016C>T
ENST00000252936.8:c.2700C>T MANE Select	ENSP00000252936.3:p.Thr900=
ENST00000417178.7:c.2310C>T	ENSP00000395666.2:p.Thr770=
ENST00000543663.6:c.2784C>T	ENSP00000446093.1:p.Thr928=
ENST00000252936.7:c.2700C>T	ENSP00000252936.3:p.Thr900=
ENST00000368562.5:c.1479C>T	ENSP00000357550.1:p.Thr493=
ENST00000368563.6:c.2700C>T	ENSP00000357551.2:p.Thr900=
ENST00000417178.6:c.2310C>T	ENSP00000395666.2:p.Thr770=
ENST00000477923.1:n.377C>T
ENST00000482278.5:c.*497C>T	ENSP00000436438.1:n.*497C>T
ENST00000543663.5:c.2784C>T	ENSP00000446093.1:p.Thr928=
NM_001256617.1:c.2784C>T	NP_001243546.1:p.Thr928=
NM_001256618.1:c.2310C>T	NP_001243547.1:p.Thr770=
NM_006659.3:c.2700C>T	NP_006650.1:p.Thr900=
NR_046330.1:n.3420C>T
NM_001256617.2:c.2784C>T	NP_001243546.1:p.Thr928=
NM_001256618.2:c.2310C>T	NP_001243547.1:p.Thr770=
NM_006659.4:c.2700C>T MANE Select	NP_006650.1:p.Thr900=
NR_046330.2:n.3420C>T