Canonical Allele Identifier: CA412181569
Gene: TUBGCP6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220772A>T , CM000684.2:g.50220772A>T GRCh38
NC_000022.10:g.50659201A>T , CM000684.1:g.50659201A>T GRCh37
NC_000022.9:g.49001328A>T NCBI36
NG_032160.1:g.29200T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3587T>A MANE Select ENSP00000248846.5:p.Ile1196Asn
ENST00000248846.9:c.3587T>A ENSP00000248846.5:p.Ile1196Asn
ENST00000439308.6:c.3587T>A ENSP00000397387.2:p.Ile1196Asn
ENST00000491449.5:n.1894T>A
ENST00000498611.5:n.3617+503T>A
NM_020461.3:c.3587T>A NP_065194.2:p.Ile1196Asn
XR_938347.1:n.4152T>A
XR_938348.1:n.3050-757T>A
XR_001755343.2:n.4156T>A
XR_001755344.2:n.4156T>A
XR_002958720.1:n.3054-757T>A
XR_938347.2:n.4156T>A
NM_020461.4:c.3587T>A MANE Select NP_065194.3:p.Ile1196Asn