Canonical Allele Identifier: CA1619407442

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32059031G= , CM000668.2:g.32059031G=	GRCh38
NC_000006.11:g.32026808G= , CM000668.1:g.32026808G=	GRCh37
NC_000006.10:g.32134786G=	NCBI36
NG_008337.2:g.55344C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.7493-641C= MANE Select	NP_001352205.1:n.7493-641C=
ENST00000644971.2:c.7493-641C= MANE Select	ENSP00000496448.1:n.7493-641C=
NM_001365276.1:c.7493-641C=	NP_001352205.1:n.7493-641C=
NM_019105.6:c.7493-641C=	NP_061978.6:n.7493-641C=
NM_019105.7:c.7493-641C=	NP_061978.6:n.7493-641C=
NM_019105.8:c.7493-641C=	NP_061978.6:n.7493-641C=
ENST00000375244.7:c.7493-641C=	ENSP00000364393.3:n.7493-641C=
ENST00000611016.2:c.653-641C=	ENSP00000483409.1:n.653-641C=
ENST00000647633.1:c.8234-641C=	ENSP00000497649.1:n.8234-641C=