Canonical Allele Identifier: CA5870975

Gene: TUB

Linked Data

• dbSNP Id: rs148091780
• ExAC: 11:8111678 T / G
• gnomAD v2: 11-8111678-T-G
• MyVariant Identifiers: chr11:g.8111678T>G (hg19) ; chr11:g.8090131T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090131T>G , CM000673.2:g.8090131T>G	GRCh38
NC_000011.9:g.8111678T>G , CM000673.1:g.8111678T>G	GRCh37
NC_000011.8:g.8068254T>G	NCBI36
NG_029912.1:g.56499T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.153T>G MANE Select	ENSP00000299506.3:p.Asn51Lys
ENST00000299506.2:c.153T>G	ENSP00000299506.2:p.Asn51Lys
ENST00000305253.8:c.318T>G	ENSP00000305426.4:p.Asn106Lys
ENST00000534099.5:c.171T>G	ENSP00000434400.1:p.Asn57Lys
NM_003320.4:c.318T>G	NP_003311.2:p.Asn106Lys
NM_177972.2:c.153T>G	NP_813977.1:p.Asn51Lys
XM_005253109.2:c.279T>G	XP_005253166.1:p.Asn93Lys
XM_011520344.1:c.189T>G	XP_011518646.1:p.Asn63Lys
XM_005253109.3:c.279T>G	XP_005253166.1:p.Asn93Lys
XM_011520344.2:c.189T>G	XP_011518646.1:p.Asn63Lys
NM_177972.3:c.153T>G MANE Select	NP_813977.1:p.Asn51Lys
NM_003320.5:c.318T>G	NP_003311.2:p.Asn106Lys