Canonical Allele Identifier: CA2612330390
Gene: TUB HGNC NCBI

Linked Data

gnomAD v4: 11-8089744-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089744C>A , CM000673.2:g.8089744C>A GRCh38
NC_000011.9:g.8111291C>A , CM000673.1:g.8111291C>A GRCh37
NC_000011.8:g.8067867C>A NCBI36
NG_029912.1:g.56112C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.90+83C>A MANE Select ENSP00000299506.3:n.90+83C>A
ENST00000299506.2:c.90+83C>A ENSP00000299506.2:n.90+83C>A
ENST00000305253.8:c.255+83C>A ENSP00000305426.4:n.255+83C>A
ENST00000534099.5:c.108+83C>A ENSP00000434400.1:n.108+83C>A
NM_003320.4:c.255+83C>A NP_003311.2:n.255+83C>A
NM_177972.2:c.90+83C>A NP_813977.1:n.90+83C>A
XM_005253109.2:c.216+83C>A XP_005253166.1:n.216+83C>A
XM_011520344.1:c.126+83C>A XP_011518646.1:n.126+83C>A
XM_005253109.3:c.216+83C>A XP_005253166.1:n.216+83C>A
XM_011520344.2:c.126+83C>A XP_011518646.1:n.126+83C>A
NM_177972.3:c.90+83C>A MANE Select NP_813977.1:n.90+83C>A
NM_003320.5:c.255+83C>A NP_003311.2:n.255+83C>A