Canonical Allele Identifier: CA1329131289

Gene: TUBA4A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219251266T= , CM000664.2:g.219251266T=	GRCh38
NC_000002.11:g.220115988T= , CM000664.1:g.220115988T=	GRCh37
NC_000002.10:g.219824232T=	NCBI36
NG_029913.1:g.7651A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006000.3:c.433A= MANE Select	NP_005991.1:p.Thr145=
ENST00000248437.9:c.433A= MANE Select	ENSP00000248437.4:p.Thr145=
NM_001278552.1:c.388A=	NP_001265481.1:p.Thr130=
NM_001278552.2:c.388A=	NP_001265481.1:p.Thr130=
NM_006000.2:c.433A=	NP_005991.1:p.Thr145=
ENST00000248437.8:c.433A=	ENSP00000248437.4:p.Thr145=
ENST00000392088.6:c.388A=	ENSP00000375938.2:p.Thr130=
ENST00000398989.2:c.-27A=	ENSP00000396212.1:n.-27A=
ENST00000427737.5:c.388A=	ENSP00000408194.1:p.Thr130=
ENST00000427737.6:c.388A=	ENSP00000408194.1:p.Thr130=
ENST00000447205.1:c.388A=	ENSP00000396061.1:p.Thr130=
ENST00000456818.5:c.502A=	ENSP00000416992.1:p.Thr168=
ENST00000462806.5:n.732A=
ENST00000498660.1:n.253A=
XM_005246832.1:c.388A=	XP_005246889.1:p.Thr130=
XM_017004824.1:c.-27A=	XP_016860313.1:n.-27A=