Canonical Allele Identifier: CA2813439740
Gene: TUBB4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6495736_6495737insACA , CM000681.2:g.6495736_6495737insACA GRCh38
NC_000019.9:g.6495747_6495748insACA , CM000681.1:g.6495747_6495748insACA GRCh37
NC_000019.8:g.6446747_6446748insACA NCBI36
NG_033896.1:g.12112_12113insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264071.7:c.762_763insTGT MANE Select ENSP00000264071.1:p.Ala254_Val255insCys
ENST00000264071.6:c.762_763insTGT ENSP00000264071.1:p.Ala254_Val255insCys
ENST00000540257.5:c.762_763insTGT ENSP00000443590.1:p.Ala254_Val255insCys
ENST00000594276.5:c.450_451insTGT ENSP00000472481.1:p.Ala150_Val151insCys
NM_001289123.1:c.915_916insTGT NP_001276052.1:p.Ala305_Val306insCys
NM_001289127.1:c.897_898insTGT NP_001276056.1:p.Ala299_Val300insCys
NM_001289129.1:c.762_763insTGT NP_001276058.1:p.Ala254_Val255insCys
NM_001289130.1:c.546_547insTGT NP_001276059.1:p.Ala182_Val183insCys
NM_001289131.1:c.546_547insTGT NP_001276060.1:p.Ala182_Val183insCys
NM_006087.3:c.762_763insTGT NP_006078.2:p.Ala254_Val255insCys
NM_006087.4:c.762_763insTGT MANE Select NP_006078.2:p.Ala254_Val255insCys
NM_001289123.2:c.915_916insTGT NP_001276052.1:p.Ala305_Val306insCys
NM_001289127.2:c.897_898insTGT NP_001276056.1:p.Ala299_Val300insCys
NM_001289129.2:c.762_763insTGT NP_001276058.1:p.Ala254_Val255insCys
NM_001289130.2:c.546_547insTGT NP_001276059.1:p.Ala182_Val183insCys
NM_001289131.2:c.546_547insTGT NP_001276060.1:p.Ala182_Val183insCys