Canonical Allele Identifier: CA344954307

Gene: B3GALNT2 TBCE

Linked Data

• MyVariant Identifiers: chr1:g.235613604G>C (hg19) ; chr1:g.235450289G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235450289G>C , CM000663.2:g.235450289G>C	GRCh38
NC_000001.10:g.235613604G>C , CM000663.1:g.235613604G>C	GRCh37
NC_000001.9:g.233680227G>C	NCBI36
NG_009230.1:g.87877G>C
NG_033219.2:g.59193C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.1420C>G (B3GALNT2) MANE Select	ENSP00000355559.3:p.Pro474Ala
ENST00000642610.2:c.*1527G>C (TBCE) MANE Select	ENSP00000494796.1:n.*1527G>C
ENST00000675193.1:c.*360C>G (B3GALNT2)	ENSP00000502069.1:n.*360C>G
ENST00000675555.1:c.1198C>G (B3GALNT2)	ENSP00000501896.1:p.Pro400Ala
ENST00000676288.1:c.*1068C>G (B3GALNT2)	ENSP00000502392.1:n.*1068C>G
ENST00000366600.7:c.1420C>G (B3GALNT2)	ENSP00000355559.3:p.Pro474Ala
NM_152490.4:c.1420C>G (B3GALNT2)	NP_689703.1:p.Pro474Ala
XM_006711749.2:c.1420C>G (B3GALNT2)	XP_006711812.1:p.Pro474Ala
XM_006711749.3:c.1420C>G (B3GALNT2)	XP_006711812.1:p.Pro474Ala
XM_017000394.1:c.1543C>G (B3GALNT2)	XP_016855883.1:p.Pro515Ala
XM_017000395.1:c.*96C>G (B3GALNT2)	XP_016855884.1:n.*96C>G
XR_001736987.1:n.1524C>G (B3GALNT2)
XR_001736989.1:n.1445C>G (B3GALNT2)
XR_001736990.1:n.1407C>G (B3GALNT2)
NM_003193.5:c.*1527G>C (TBCE) MANE Select	NP_003184.1:n.*1527G>C
NM_152490.5:c.1420C>G (B3GALNT2) MANE Select	NP_689703.1:p.Pro474Ala
NM_001079515.3:c.*1527G>C (TBCE)	NP_001072983.1:n.*1527G>C
NM_001287801.2:c.*1527G>C (TBCE)	NP_001274730.1:n.*1527G>C
NM_001287802.2:c.*1527G>C (TBCE)	NP_001274731.1:n.*1527G>C