Canonical Allele Identifier: CA515377067

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50662947T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50224518T>G , CM000684.2:g.50224518T>G	GRCh38
NC_000022.10:g.50662947T>G , CM000684.1:g.50662947T>G	GRCh37
NC_000022.9:g.49005074T>G	NCBI36
NG_032160.1:g.25454A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248846.10:c.2058A>C MANE Select	ENSP00000248846.5:p.Ala686=
ENST00000248846.9:c.2058A>C	ENSP00000248846.5:p.Ala686=
ENST00000439308.6:c.2058A>C	ENSP00000397387.2:p.Ala686=
ENST00000473946.1:n.367A>C
ENST00000489511.5:n.75A>C
ENST00000491449.5:n.365A>C
ENST00000498611.5:n.2591A>C
NM_020461.3:c.2058A>C	NP_065194.2:p.Ala686=
XR_938347.1:n.2623A>C
XR_938348.1:n.2623A>C
XR_001755343.2:n.2627A>C
XR_001755344.2:n.2627A>C
XR_002958720.1:n.2627A>C
XR_938347.2:n.2627A>C
NM_020461.4:c.2058A>C MANE Select	NP_065194.3:p.Ala686=