Canonical Allele Identifier: CA412182000

Gene: TUBGCP6

Linked Data

• gnomAD v4: 22-50220842-C-T
• MyVariant Identifiers: chr22:g.50659271C>T (hg19) ; chr22:g.50220842C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220842C>T , CM000684.2:g.50220842C>T	GRCh38
NC_000022.10:g.50659271C>T , CM000684.1:g.50659271C>T	GRCh37
NC_000022.9:g.49001398C>T	NCBI36
NG_032160.1:g.29130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3517G>A MANE Select	ENSP00000248846.5:p.Glu1173Lys
ENST00000248846.9:c.3517G>A	ENSP00000248846.5:p.Glu1173Lys
ENST00000439308.6:c.3517G>A	ENSP00000397387.2:p.Glu1173Lys
ENST00000491449.5:n.1824G>A
ENST00000498611.5:n.3617+433G>A
NM_020461.3:c.3517G>A	NP_065194.2:p.Glu1173Lys
XR_938347.1:n.4082G>A
XR_938348.1:n.3050-827G>A
XR_001755343.2:n.4086G>A
XR_001755344.2:n.4086G>A
XR_002958720.1:n.3054-827G>A
XR_938347.2:n.4086G>A
NM_020461.4:c.3517G>A MANE Select	NP_065194.3:p.Glu1173Lys