Canonical Allele Identifier: CA379562894

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111706G>T (hg19) ; chr11:g.8090159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090159G>T , CM000673.2:g.8090159G>T	GRCh38
NC_000011.9:g.8111706G>T , CM000673.1:g.8111706G>T	GRCh37
NC_000011.8:g.8068282G>T	NCBI36
NG_029912.1:g.56527G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.181G>T MANE Select	ENSP00000299506.3:p.Ala61Ser
ENST00000299506.2:c.181G>T	ENSP00000299506.2:p.Ala61Ser
ENST00000305253.8:c.346G>T	ENSP00000305426.4:p.Ala116Ser
ENST00000534099.5:c.199G>T	ENSP00000434400.1:p.Ala67Ser
NM_003320.4:c.346G>T	NP_003311.2:p.Ala116Ser
NM_177972.2:c.181G>T	NP_813977.1:p.Ala61Ser
XM_005253109.2:c.307G>T	XP_005253166.1:p.Ala103Ser
XM_011520344.1:c.217G>T	XP_011518646.1:p.Ala73Ser
XM_005253109.3:c.307G>T	XP_005253166.1:p.Ala103Ser
XM_011520344.2:c.217G>T	XP_011518646.1:p.Ala73Ser
NM_177972.3:c.181G>T MANE Select	NP_813977.1:p.Ala61Ser
NM_003320.5:c.346G>T	NP_003311.2:p.Ala116Ser