Canonical Allele Identifier: CA344954322

Gene: B3GALNT2 TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235613609G>A (hg19) ; chr1:g.235450294G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235450294G>A , CM000663.2:g.235450294G>A	GRCh38
NC_000001.10:g.235613609G>A , CM000663.1:g.235613609G>A	GRCh37
NC_000001.9:g.233680232G>A	NCBI36
NG_009230.1:g.87882G>A
NG_033219.2:g.59188C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.1415C>T (B3GALNT2) MANE Select	ENSP00000355559.3:p.Ser472Phe
ENST00000642610.2:c.*1532G>A (TBCE) MANE Select	ENSP00000494796.1:n.*1532G>A
ENST00000675193.1:c.*355C>T (B3GALNT2)	ENSP00000502069.1:n.*355C>T
ENST00000675555.1:c.1193C>T (B3GALNT2)	ENSP00000501896.1:p.Ser398Phe
ENST00000676288.1:c.*1063C>T (B3GALNT2)	ENSP00000502392.1:n.*1063C>T
ENST00000366600.7:c.1415C>T (B3GALNT2)	ENSP00000355559.3:p.Ser472Phe
NM_152490.4:c.1415C>T (B3GALNT2)	NP_689703.1:p.Ser472Phe
XM_006711749.2:c.1415C>T (B3GALNT2)	XP_006711812.1:p.Ser472Phe
XM_006711749.3:c.1415C>T (B3GALNT2)	XP_006711812.1:p.Ser472Phe
XM_017000394.1:c.1538C>T (B3GALNT2)	XP_016855883.1:p.Ser513Phe
XM_017000395.1:c.*91C>T (B3GALNT2)	XP_016855884.1:n.*91C>T
XR_001736987.1:n.1519C>T (B3GALNT2)
XR_001736989.1:n.1440C>T (B3GALNT2)
XR_001736990.1:n.1402C>T (B3GALNT2)
NM_003193.5:c.*1532G>A (TBCE) MANE Select	NP_003184.1:n.*1532G>A
NM_152490.5:c.1415C>T (B3GALNT2) MANE Select	NP_689703.1:p.Ser472Phe
NM_001079515.3:c.*1532G>A (TBCE)	NP_001072983.1:n.*1532G>A
NM_001287801.2:c.*1532G>A (TBCE)	NP_001274730.1:n.*1532G>A
NM_001287802.2:c.*1532G>A (TBCE)	NP_001274731.1:n.*1532G>A