Canonical Allele Identifier: CA505189940
Gene: TUBB4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6495790C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6495779C>T , CM000681.2:g.6495779C>T GRCh38
NC_000019.9:g.6495790C>T , CM000681.1:g.6495790C>T GRCh37
NC_000019.8:g.6446790C>T NCBI36
NG_033896.1:g.12070G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264071.7:c.720G>A MANE Select ENSP00000264071.1:p.Leu240=
ENST00000264071.6:c.720G>A ENSP00000264071.1:p.Leu240=
ENST00000540257.5:c.720G>A ENSP00000443590.1:p.Leu240=
ENST00000594276.5:c.408G>A ENSP00000472481.1:p.Leu136=
NM_001289123.1:c.873G>A NP_001276052.1:p.Leu291=
NM_001289127.1:c.855G>A NP_001276056.1:p.Leu285=
NM_001289129.1:c.720G>A NP_001276058.1:p.Leu240=
NM_001289130.1:c.504G>A NP_001276059.1:p.Leu168=
NM_001289131.1:c.504G>A NP_001276060.1:p.Leu168=
NM_006087.3:c.720G>A NP_006078.2:p.Leu240=
NM_006087.4:c.720G>A MANE Select NP_006078.2:p.Leu240=
NM_001289123.2:c.873G>A NP_001276052.1:p.Leu291=
NM_001289127.2:c.855G>A NP_001276056.1:p.Leu285=
NM_001289129.2:c.720G>A NP_001276058.1:p.Leu240=
NM_001289130.2:c.504G>A NP_001276059.1:p.Leu168=
NM_001289131.2:c.504G>A NP_001276060.1:p.Leu168=