Canonical Allele Identifier: CA412181490
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs745971353

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220758A>C , CM000684.2:g.50220758A>C GRCh38
NC_000022.10:g.50659187A>C , CM000684.1:g.50659187A>C GRCh37
NC_000022.9:g.49001314A>C NCBI36
NG_032160.1:g.29214T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3601T>G MANE Select ENSP00000248846.5:p.Ser1201Ala
ENST00000248846.9:c.3601T>G ENSP00000248846.5:p.Ser1201Ala
ENST00000439308.6:c.3601T>G ENSP00000397387.2:p.Ser1201Ala
ENST00000491449.5:n.1908T>G
ENST00000498611.5:n.3617+517T>G
NM_020461.3:c.3601T>G NP_065194.2:p.Ser1201Ala
XR_938347.1:n.4166T>G
XR_938348.1:n.3050-743T>G
XR_001755343.2:n.4170T>G
XR_001755344.2:n.4170T>G
XR_002958720.1:n.3054-743T>G
XR_938347.2:n.4170T>G
NM_020461.4:c.3601T>G MANE Select NP_065194.3:p.Ser1201Ala