Canonical Allele Identifier: CA515376518

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50659701C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50221272C>G , CM000684.2:g.50221272C>G	GRCh38
NC_000022.10:g.50659701C>G , CM000684.1:g.50659701C>G	GRCh37
NC_000022.9:g.49001828C>G	NCBI36
NG_032160.1:g.28700G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3087G>C MANE Select	ENSP00000248846.5:p.Val1029=
ENST00000248846.9:c.3087G>C	ENSP00000248846.5:p.Val1029=
ENST00000439308.6:c.3087G>C	ENSP00000397387.2:p.Val1029=
ENST00000491449.5:n.1394G>C
ENST00000498611.5:n.3617+3G>C
NM_020461.3:c.3087G>C	NP_065194.2:p.Val1029=
XR_938347.1:n.3652G>C
XR_938348.1:n.3049+756G>C
XR_001755343.2:n.3656G>C
XR_001755344.2:n.3656G>C
XR_002958720.1:n.3053+756G>C
XR_938347.2:n.3656G>C
NM_020461.4:c.3087G>C MANE Select	NP_065194.3:p.Val1029=