Canonical Allele Identifier: CA365997025

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378729C>T , CM000668.2:g.149378729C>T	GRCh38
NC_000006.11:g.149699865C>T , CM000668.1:g.149699865C>T	GRCh37
NC_000006.10:g.149741558C>T	NCBI36
NG_021386.1:g.65430C>T
NG_021386.2:g.165806C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001292034.3:c.814C>T MANE Select	NP_001278963.1:p.Gln272Ter
ENST00000637181.2:c.814C>T MANE Select	ENSP00000490618.1:p.Gln272Ter
NM_001292034.2:c.814C>T	NP_001278963.1:p.Gln272Ter
NM_001292035.2:c.718C>T	NP_001278964.1:p.Gln240Ter
NM_001292035.3:c.718C>T	NP_001278964.1:p.Gln240Ter
NM_001369506.1:c.814C>T	NP_001356435.1:p.Gln272Ter
NM_015093.5:c.814C>T	NP_055908.1:p.Gln272Ter
NM_015093.6:c.814C>T	NP_055908.1:p.Gln272Ter
ENST00000367456.5:c.814C>T	ENSP00000356426.1:p.Gln272Ter
ENST00000470466.5:c.814C>T	ENSP00000432709.1:p.Gln272Ter
ENST00000538427.5:c.814C>T	ENSP00000445752.1:p.Gln272Ter
ENST00000636456.1:c.-39C>T	ENSP00000490379.1:n.-39C>T
ENST00000703212.1:n.1229C>T
ENST00000703213.1:c.814C>T	ENSP00000515239.1:p.Gln272Ter
XM_006715403.2:c.814C>T	XP_006715466.1:p.Gln272Ter
XM_011535633.1:c.814C>T	XP_011533935.1:p.Gln272Ter
XM_011535633.2:c.814C>T	XP_011533935.1:p.Gln272Ter
XM_011535634.1:c.814C>T	XP_011533936.1:p.Gln272Ter
XM_017010591.1:c.814C>T	XP_016866080.1:p.Gln272Ter
XM_017010592.2:c.814C>T	XP_016866081.1:p.Gln272Ter