Canonical Allele Identifier: CA505189931

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495787G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495776G>C , CM000681.2:g.6495776G>C	GRCh38
NC_000019.9:g.6495787G>C , CM000681.1:g.6495787G>C	GRCh37
NC_000019.8:g.6446787G>C	NCBI36
NG_033896.1:g.12073C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.723C>G MANE Select	ENSP00000264071.1:p.Arg241=
ENST00000264071.6:c.723C>G	ENSP00000264071.1:p.Arg241=
ENST00000540257.5:c.723C>G	ENSP00000443590.1:p.Arg241=
ENST00000594276.5:c.411C>G	ENSP00000472481.1:p.Arg137=
NM_001289123.1:c.876C>G	NP_001276052.1:p.Arg292=
NM_001289127.1:c.858C>G	NP_001276056.1:p.Arg286=
NM_001289129.1:c.723C>G	NP_001276058.1:p.Arg241=
NM_001289130.1:c.507C>G	NP_001276059.1:p.Arg169=
NM_001289131.1:c.507C>G	NP_001276060.1:p.Arg169=
NM_006087.3:c.723C>G	NP_006078.2:p.Arg241=
NM_006087.4:c.723C>G MANE Select	NP_006078.2:p.Arg241=
NM_001289123.2:c.876C>G	NP_001276052.1:p.Arg292=
NM_001289127.2:c.858C>G	NP_001276056.1:p.Arg286=
NM_001289129.2:c.723C>G	NP_001276058.1:p.Arg241=
NM_001289130.2:c.507C>G	NP_001276059.1:p.Arg169=
NM_001289131.2:c.507C>G	NP_001276060.1:p.Arg169=