Canonical Allele Identifier: CA412184013
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs138868325

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221099C>G , CM000684.2:g.50221099C>G GRCh38
NC_000022.10:g.50659528C>G , CM000684.1:g.50659528C>G GRCh37
NC_000022.9:g.49001655C>G NCBI36
NG_032160.1:g.28873G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3260G>C MANE Select ENSP00000248846.5:p.Ser1087Thr
ENST00000248846.9:c.3260G>C ENSP00000248846.5:p.Ser1087Thr
ENST00000439308.6:c.3260G>C ENSP00000397387.2:p.Ser1087Thr
ENST00000491449.5:n.1567G>C
ENST00000498611.5:n.3617+176G>C
NM_020461.3:c.3260G>C NP_065194.2:p.Ser1087Thr
XR_938347.1:n.3825G>C
XR_938348.1:n.3049+929G>C
XR_001755343.2:n.3829G>C
XR_001755344.2:n.3829G>C
XR_002958720.1:n.3053+929G>C
XR_938347.2:n.3829G>C
NM_020461.4:c.3260G>C MANE Select NP_065194.3:p.Ser1087Thr