Canonical Allele Identifier: CA3733477

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32049443G>A , CM000668.2:g.32049443G>A	GRCh38
NC_000006.11:g.32017220G>A , CM000668.1:g.32017220G>A	GRCh37
NC_000006.10:g.32125198G>A	NCBI36
NG_008337.2:g.64932C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.9584C>T MANE Select	NP_001352205.1:p.Ser3195Phe
ENST00000644971.2:c.9584C>T MANE Select	ENSP00000496448.1:p.Ser3195Phe
NM_001365276.1:c.9584C>T	NP_001352205.1:p.Ser3195Phe
NM_019105.6:c.9578C>T	NP_061978.6:p.Ser3193Phe
NM_019105.7:c.9578C>T	NP_061978.6:p.Ser3193Phe
NM_019105.8:c.9578C>T	NP_061978.6:p.Ser3193Phe
ENST00000375244.7:c.9584C>T	ENSP00000364393.3:p.Ser3195Phe
ENST00000611016.2:c.2738C>T	ENSP00000483409.1:p.Ser913Phe
ENST00000647633.1:c.10325C>T	ENSP00000497649.1:p.Ser3442Phe