Canonical Allele Identifier: CA412178067

Gene: TUBGCP6

Linked Data

• gnomAD v4: 22-50220487-G-T
• MyVariant Identifiers: chr22:g.50658916G>T (hg19) ; chr22:g.50220487G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220487G>T , CM000684.2:g.50220487G>T	GRCh38
NC_000022.10:g.50658916G>T , CM000684.1:g.50658916G>T	GRCh37
NC_000022.9:g.49001043G>T	NCBI36
NG_032160.1:g.29485C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3872C>A MANE Select	ENSP00000248846.5:p.Pro1291His
ENST00000248846.9:c.3872C>A	ENSP00000248846.5:p.Pro1291His
ENST00000439308.6:c.3872C>A	ENSP00000397387.2:p.Pro1291His
ENST00000491449.5:n.2179C>A
ENST00000498611.5:n.3618-472C>A
NM_020461.3:c.3872C>A	NP_065194.2:p.Pro1291His
XR_938347.1:n.4437C>A
XR_938348.1:n.3050-472C>A
XR_001755343.2:n.4441C>A
XR_001755344.2:n.4441C>A
XR_002958720.1:n.3054-472C>A
XR_938347.2:n.4441C>A
NM_020461.4:c.3872C>A MANE Select	NP_065194.3:p.Pro1291His