Canonical Allele Identifier: CA379562667
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090101G>C , CM000673.2:g.8090101G>C GRCh38
NC_000011.9:g.8111648G>C , CM000673.1:g.8111648G>C GRCh37
NC_000011.8:g.8068224G>C NCBI36
NG_029912.1:g.56469G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.123G>C MANE Select ENSP00000299506.3:p.Lys41Asn
ENST00000299506.2:c.123G>C ENSP00000299506.2:p.Lys41Asn
ENST00000305253.8:c.288G>C ENSP00000305426.4:p.Lys96Asn
ENST00000534099.5:c.141G>C ENSP00000434400.1:p.Lys47Asn
NM_003320.4:c.288G>C NP_003311.2:p.Lys96Asn
NM_177972.2:c.123G>C NP_813977.1:p.Lys41Asn
XM_005253109.2:c.249G>C XP_005253166.1:p.Lys83Asn
XM_011520344.1:c.159G>C XP_011518646.1:p.Lys53Asn
XM_005253109.3:c.249G>C XP_005253166.1:p.Lys83Asn
XM_011520344.2:c.159G>C XP_011518646.1:p.Lys53Asn
NM_177972.3:c.123G>C MANE Select NP_813977.1:p.Lys41Asn
NM_003320.5:c.288G>C NP_003311.2:p.Lys96Asn