Canonical Allele Identifier: CA505189563

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495823C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495812C>T , CM000681.2:g.6495812C>T	GRCh38
NC_000019.9:g.6495823C>T , CM000681.1:g.6495823C>T	GRCh37
NC_000019.8:g.6446823C>T	NCBI36
NG_033896.1:g.12037G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.687G>A MANE Select	ENSP00000264071.1:p.Val229=
ENST00000264071.6:c.687G>A	ENSP00000264071.1:p.Val229=
ENST00000540257.5:c.687G>A	ENSP00000443590.1:p.Val229=
ENST00000594075.5:c.477G>A	ENSP00000469936.1:p.Val159=
ENST00000594276.5:c.375G>A	ENSP00000472481.1:p.Val125=
ENST00000600216.5:c.429G>A	ENSP00000470983.1:p.Val143=
NM_001289123.1:c.840G>A	NP_001276052.1:p.Val280=
NM_001289127.1:c.822G>A	NP_001276056.1:p.Val274=
NM_001289129.1:c.687G>A	NP_001276058.1:p.Val229=
NM_001289130.1:c.471G>A	NP_001276059.1:p.Val157=
NM_001289131.1:c.471G>A	NP_001276060.1:p.Val157=
NM_006087.3:c.687G>A	NP_006078.2:p.Val229=
NM_006087.4:c.687G>A MANE Select	NP_006078.2:p.Val229=
NM_001289123.2:c.840G>A	NP_001276052.1:p.Val280=
NM_001289127.2:c.822G>A	NP_001276056.1:p.Val274=
NM_001289129.2:c.687G>A	NP_001276058.1:p.Val229=
NM_001289130.2:c.471G>A	NP_001276059.1:p.Val157=
NM_001289131.2:c.471G>A	NP_001276060.1:p.Val157=