Canonical Allele Identifier: CA505189873

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495763G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495752G>A , CM000681.2:g.6495752G>A	GRCh38
NC_000019.9:g.6495763G>A , CM000681.1:g.6495763G>A	GRCh37
NC_000019.8:g.6446763G>A	NCBI36
NG_033896.1:g.12097C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.747C>T MANE Select	ENSP00000264071.1:p.Asp249=
ENST00000264071.6:c.747C>T	ENSP00000264071.1:p.Asp249=
ENST00000540257.5:c.747C>T	ENSP00000443590.1:p.Asp249=
ENST00000594276.5:c.435C>T	ENSP00000472481.1:p.Asp145=
NM_001289123.1:c.900C>T	NP_001276052.1:p.Asp300=
NM_001289127.1:c.882C>T	NP_001276056.1:p.Asp294=
NM_001289129.1:c.747C>T	NP_001276058.1:p.Asp249=
NM_001289130.1:c.531C>T	NP_001276059.1:p.Asp177=
NM_001289131.1:c.531C>T	NP_001276060.1:p.Asp177=
NM_006087.3:c.747C>T	NP_006078.2:p.Asp249=
NM_006087.4:c.747C>T MANE Select	NP_006078.2:p.Asp249=
NM_001289123.2:c.900C>T	NP_001276052.1:p.Asp300=
NM_001289127.2:c.882C>T	NP_001276056.1:p.Asp294=
NM_001289129.2:c.747C>T	NP_001276058.1:p.Asp249=
NM_001289130.2:c.531C>T	NP_001276059.1:p.Asp177=
NM_001289131.2:c.531C>T	NP_001276060.1:p.Asp177=