Canonical Allele Identifier: CA733125874
Gene: B3GALNT2 HGNC NCBI

Linked Data

dbSNP Id: rs1339697305

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235489067_235489079del , CM000663.2:g.235489067_235489079del GRCh38
NC_000001.10:g.235652372_235652384del , CM000663.1:g.235652372_235652384del GRCh37
NC_000001.9:g.233718995_233719007del NCBI36
NG_033219.2:g.20412_20424del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366600.8:c.361+98_361+110del MANE Select ENSP00000355559.3:n.361+98_361+110del
ENST00000675193.1:c.484+98_484+110del ENSP00000502069.1:n.484+98_484+110del
ENST00000675555.1:c.139+98_139+110del ENSP00000501896.1:n.139+98_139+110del
ENST00000676288.1:c.484+98_484+110del ENSP00000502392.1:n.484+98_484+110del
ENST00000313984.3:c.484+98_484+110del ENSP00000315678.3:n.484+98_484+110del
ENST00000366600.7:c.361+98_361+110del ENSP00000355559.3:n.361+98_361+110del
ENST00000494378.1:n.434-4555_434-4543del
ENST00000612859.4:c.261-4555_261-4543del ENSP00000481548.1:n.261-4555_261-4543del
NM_001277155.2:c.484+98_484+110del NP_001264084.1:n.484+98_484+110del
NM_152490.4:c.361+98_361+110del NP_689703.1:n.361+98_361+110del
XM_005273071.3:c.361+98_361+110del XP_005273128.1:n.361+98_361+110del
XM_006711749.2:c.361+98_361+110del XP_006711812.1:n.361+98_361+110del
XM_011544096.1:c.361+98_361+110del XP_011542398.1:n.361+98_361+110del
XM_011544097.1:c.361+98_361+110del XP_011542399.1:n.361+98_361+110del
XM_006711749.3:c.361+98_361+110del XP_006711812.1:n.361+98_361+110del
XM_017000394.1:c.484+98_484+110del XP_016855883.1:n.484+98_484+110del
XM_017000395.1:c.484+98_484+110del XP_016855884.1:n.484+98_484+110del
XR_001736987.1:n.649+98_649+110del
XR_001736988.1:n.649+98_649+110del
XR_001736989.1:n.649+98_649+110del
XR_001736990.1:n.532+98_532+110del
NM_152490.5:c.361+98_361+110del MANE Select NP_689703.1:n.361+98_361+110del
NM_001277155.3:c.484+98_484+110del NP_001264084.1:n.484+98_484+110del