Canonical Allele Identifier: CA4199724

Gene: TAX1BP1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27792112A>C , CM000669.2:g.27792112A>C	GRCh38
NC_000007.13:g.27831731A>C , CM000669.1:g.27831731A>C	GRCh37
NC_000007.12:g.27798256A>C	NCBI36
NG_029523.1:g.57740A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006024.7:c.1145A>C MANE Select	NP_006015.4:p.Asn382Thr
ENST00000396319.7:c.1145A>C MANE Select	ENSP00000379612.2:p.Asn382Thr
NM_001079864.2:c.1145A>C	NP_001073333.1:p.Asn382Thr
NM_001079864.3:c.1145A>C	NP_001073333.1:p.Asn382Thr
NM_001206901.1:c.1145A>C	NP_001193830.1:p.Asn382Thr
NM_001206902.1:c.674A>C	NP_001193831.1:p.Asn225Thr
NM_001206902.2:c.674A>C	NP_001193831.1:p.Asn225Thr
NM_001362794.1:c.1145A>C	NP_001349723.1:p.Asn382Thr
NM_001362794.2:c.1145A>C	NP_001349723.1:p.Asn382Thr
NM_001362795.1:c.1145A>C	NP_001349724.1:p.Asn382Thr
NM_001362795.2:c.1145A>C	NP_001349724.1:p.Asn382Thr
NM_006024.6:c.1145A>C	NP_006015.4:p.Asn382Thr
ENST00000265393.10:c.1145A>C	ENSP00000265393.6:p.Asn382Thr
ENST00000396319.6:c.1145A>C	ENSP00000379612.2:p.Asn382Thr
ENST00000409980.5:c.1145A>C	ENSP00000386515.1:p.Asn382Thr
ENST00000416801.6:c.*681A>C	ENSP00000391215.2:n.*681A>C
ENST00000433216.6:c.674A>C	ENSP00000391907.2:p.Asn225Thr
ENST00000543117.5:c.1145A>C	ENSP00000444811.1:p.Asn382Thr
XM_005249900.1:c.1145A>C	XP_005249957.1:p.Asn382Thr