Canonical Allele Identifier: CA505189860

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495757G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495746G>T , CM000681.2:g.6495746G>T	GRCh38
NC_000019.9:g.6495757G>T , CM000681.1:g.6495757G>T	GRCh37
NC_000019.8:g.6446757G>T	NCBI36
NG_033896.1:g.12103C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.753C>A MANE Select	ENSP00000264071.1:p.Arg251=
ENST00000264071.6:c.753C>A	ENSP00000264071.1:p.Arg251=
ENST00000540257.5:c.753C>A	ENSP00000443590.1:p.Arg251=
ENST00000594276.5:c.441C>A	ENSP00000472481.1:p.Arg147=
NM_001289123.1:c.906C>A	NP_001276052.1:p.Arg302=
NM_001289127.1:c.888C>A	NP_001276056.1:p.Arg296=
NM_001289129.1:c.753C>A	NP_001276058.1:p.Arg251=
NM_001289130.1:c.537C>A	NP_001276059.1:p.Arg179=
NM_001289131.1:c.537C>A	NP_001276060.1:p.Arg179=
NM_006087.3:c.753C>A	NP_006078.2:p.Arg251=
NM_006087.4:c.753C>A MANE Select	NP_006078.2:p.Arg251=
NM_001289123.2:c.906C>A	NP_001276052.1:p.Arg302=
NM_001289127.2:c.888C>A	NP_001276056.1:p.Arg296=
NM_001289129.2:c.753C>A	NP_001276058.1:p.Arg251=
NM_001289130.2:c.537C>A	NP_001276059.1:p.Arg179=
NM_001289131.2:c.537C>A	NP_001276060.1:p.Arg179=