Canonical Allele Identifier: CA412102873
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50662774A>T (hg19) chr22:g.50224345A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50224345A>T , CM000684.2:g.50224345A>T GRCh38
NC_000022.10:g.50662774A>T , CM000684.1:g.50662774A>T GRCh37
NC_000022.9:g.49004901A>T NCBI36
NG_032160.1:g.25627T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.2141T>A MANE Select ENSP00000248846.5:p.Val714Glu
ENST00000248846.9:c.2141T>A ENSP00000248846.5:p.Val714Glu
ENST00000439308.6:c.2141T>A ENSP00000397387.2:p.Val714Glu
ENST00000473946.1:n.450T>A
ENST00000489511.5:n.158T>A
ENST00000491449.5:n.448T>A
ENST00000498611.5:n.2674T>A
NM_020461.3:c.2141T>A NP_065194.2:p.Val714Glu
XR_938347.1:n.2706T>A
XR_938348.1:n.2706T>A
XR_001755343.2:n.2710T>A
XR_001755344.2:n.2710T>A
XR_002958720.1:n.2710T>A
XR_938347.2:n.2710T>A
NM_020461.4:c.2141T>A MANE Select NP_065194.3:p.Val714Glu
Search 100 bp 5'
Search 100 bp 3'