Canonical Allele Identifier: CA1619416851

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32082296G= , CM000668.2:g.32082296G=	GRCh38
NC_000006.11:g.32050073G= , CM000668.1:g.32050073G=	GRCh37
NC_000006.10:g.32158051G=	NCBI36
NG_008337.2:g.32079C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644971.2:c.3476C= MANE Select	ENSP00000496448.1:p.Pro1159=
ENST00000647633.1:c.4217C=	ENSP00000497649.1:p.Pro1406=
ENST00000375244.7:c.3476C=	ENSP00000364393.3:p.Pro1159=
ENST00000613214.4:c.3737C=	ENSP00000480067.1:p.Pro1246=
NM_019105.6:c.3476C=	NP_061978.6:p.Pro1159=
NM_001365276.1:c.3476C=	NP_001352205.1:p.Pro1159=
NM_019105.7:c.3476C=	NP_061978.6:p.Pro1159=
NM_001365276.2:c.3476C= MANE Select	NP_001352205.1:p.Pro1159=
NM_019105.8:c.3476C=	NP_061978.6:p.Pro1159=