Canonical Allele Identifier: CA344954410

Gene: B3GALNT2 TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235613631T>A (hg19) ; chr1:g.235450316T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235450316T>A , CM000663.2:g.235450316T>A	GRCh38
NC_000001.10:g.235613631T>A , CM000663.1:g.235613631T>A	GRCh37
NC_000001.9:g.233680254T>A	NCBI36
NG_009230.1:g.87904T>A
NG_033219.2:g.59166A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.1393A>T (B3GALNT2) MANE Select	ENSP00000355559.3:p.Thr465Ser
ENST00000642610.2:c.*1554T>A (TBCE) MANE Select	ENSP00000494796.1:n.*1554T>A
ENST00000675193.1:c.*333A>T (B3GALNT2)	ENSP00000502069.1:n.*333A>T
ENST00000675555.1:c.1171A>T (B3GALNT2)	ENSP00000501896.1:p.Thr391Ser
ENST00000676288.1:c.*1041A>T (B3GALNT2)	ENSP00000502392.1:n.*1041A>T
ENST00000366600.7:c.1393A>T (B3GALNT2)	ENSP00000355559.3:p.Thr465Ser
NM_152490.4:c.1393A>T (B3GALNT2)	NP_689703.1:p.Thr465Ser
XM_006711749.2:c.1393A>T (B3GALNT2)	XP_006711812.1:p.Thr465Ser
XM_006711749.3:c.1393A>T (B3GALNT2)	XP_006711812.1:p.Thr465Ser
XM_017000394.1:c.1516A>T (B3GALNT2)	XP_016855883.1:p.Thr506Ser
XM_017000395.1:c.*69A>T (B3GALNT2)	XP_016855884.1:n.*69A>T
XR_001736987.1:n.1497A>T (B3GALNT2)
XR_001736989.1:n.1418A>T (B3GALNT2)
XR_001736990.1:n.1380A>T (B3GALNT2)
NM_003193.5:c.*1554T>A (TBCE) MANE Select	NP_003184.1:n.*1554T>A
NM_152490.5:c.1393A>T (B3GALNT2) MANE Select	NP_689703.1:p.Thr465Ser
NM_001079515.3:c.*1554T>A (TBCE)	NP_001072983.1:n.*1554T>A
NM_001287801.2:c.*1554T>A (TBCE)	NP_001274730.1:n.*1554T>A
NM_001287802.2:c.*1554T>A (TBCE)	NP_001274731.1:n.*1554T>A