Canonical Allele Identifier: CA16603586

Gene: B3GALNT2 TBCE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235450239C>G , CM000663.2:g.235450239C>G	GRCh38
NC_000001.10:g.235613554C>G , CM000663.1:g.235613554C>G	GRCh37
NC_000001.9:g.233680177C>G	NCBI36
NG_009230.1:g.87827C>G
NG_033219.2:g.59243G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.1470G>C (B3GALNT2) MANE Select	ENSP00000355559.3:p.Arg490=
ENST00000642610.2:c.*1477C>G (TBCE) MANE Select	ENSP00000494796.1:n.*1477C>G
ENST00000675193.1:c.*410G>C (B3GALNT2)	ENSP00000502069.1:n.*410G>C
ENST00000675555.1:c.1248G>C (B3GALNT2)	ENSP00000501896.1:p.Arg416=
ENST00000676288.1:c.*1118G>C (B3GALNT2)	ENSP00000502392.1:n.*1118G>C
ENST00000366600.7:c.1470G>C (B3GALNT2)	ENSP00000355559.3:p.Arg490=
NM_152490.4:c.1470G>C (B3GALNT2)	NP_689703.1:p.Arg490=
XM_006711749.2:c.1469+1G>C (B3GALNT2)	XP_006711812.1:n.1469+1G>C
XM_006711749.3:c.1469+1G>C (B3GALNT2)	XP_006711812.1:n.1469+1G>C
XM_017000394.1:c.1593G>C (B3GALNT2)	XP_016855883.1:p.Arg531=
XM_017000395.1:c.*146G>C (B3GALNT2)	XP_016855884.1:n.*146G>C
XR_001736987.1:n.1574G>C (B3GALNT2)
XR_001736989.1:n.1495G>C (B3GALNT2)
XR_001736990.1:n.1457G>C (B3GALNT2)
NM_003193.5:c.*1477C>G (TBCE) MANE Select	NP_003184.1:n.*1477C>G
NM_152490.5:c.1470G>C (B3GALNT2) MANE Select	NP_689703.1:p.Arg490=
NM_001079515.3:c.*1477C>G (TBCE)	NP_001072983.1:n.*1477C>G
NM_001287801.2:c.*1477C>G (TBCE)	NP_001274730.1:n.*1477C>G
NM_001287802.2:c.*1477C>G (TBCE)	NP_001274731.1:n.*1477C>G