Canonical Allele Identifier: CA412184812
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs2147179435

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221243T>A , CM000684.2:g.50221243T>A GRCh38
NC_000022.10:g.50659672T>A , CM000684.1:g.50659672T>A GRCh37
NC_000022.9:g.49001799T>A NCBI36
NG_032160.1:g.28729A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3116A>T MANE Select ENSP00000248846.5:p.Tyr1039Phe
ENST00000248846.9:c.3116A>T ENSP00000248846.5:p.Tyr1039Phe
ENST00000439308.6:c.3116A>T ENSP00000397387.2:p.Tyr1039Phe
ENST00000491449.5:n.1423A>T
ENST00000498611.5:n.3617+32A>T
NM_020461.3:c.3116A>T NP_065194.2:p.Tyr1039Phe
XR_938347.1:n.3681A>T
XR_938348.1:n.3049+785A>T
XR_001755343.2:n.3685A>T
XR_001755344.2:n.3685A>T
XR_002958720.1:n.3053+785A>T
XR_938347.2:n.3685A>T
NM_020461.4:c.3116A>T MANE Select NP_065194.3:p.Tyr1039Phe