Canonical Allele Identifier: CA1140589796
Gene: B3GALNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235489094_235489095delinsCC , CM000663.2:g.235489094_235489095delinsCC GRCh38
NC_000001.10:g.235652399_235652400delinsCC , CM000663.1:g.235652399_235652400delinsCC GRCh37
NC_000001.9:g.233719022_233719023delinsCC NCBI36
NG_033219.2:g.20387_20388delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366600.8:c.361+73_361+74delinsGG MANE Select ENSP00000355559.3:n.361+73_361+74delinsGG
ENST00000675193.1:c.484+73_484+74delinsGG ENSP00000502069.1:n.484+73_484+74delinsGG
ENST00000675555.1:c.139+73_139+74delinsGG ENSP00000501896.1:n.139+73_139+74delinsGG
ENST00000676288.1:c.484+73_484+74delinsGG ENSP00000502392.1:n.484+73_484+74delinsGG
ENST00000313984.3:c.484+73_484+74delinsGG ENSP00000315678.3:n.484+73_484+74delinsGG
ENST00000366600.7:c.361+73_361+74delinsGG ENSP00000355559.3:n.361+73_361+74delinsGG
ENST00000494378.1:n.434-4580_434-4579delinsGG
ENST00000612859.4:c.261-4580_261-4579delinsGG ENSP00000481548.1:n.261-4580_261-4579delinsGG
NM_001277155.2:c.484+73_484+74delinsGG NP_001264084.1:n.484+73_484+74delinsGG
NM_152490.4:c.361+73_361+74delinsGG NP_689703.1:n.361+73_361+74delinsGG
XM_005273071.3:c.361+73_361+74delinsGG XP_005273128.1:n.361+73_361+74delinsGG
XM_006711749.2:c.361+73_361+74delinsGG XP_006711812.1:n.361+73_361+74delinsGG
XM_011544096.1:c.361+73_361+74delinsGG XP_011542398.1:n.361+73_361+74delinsGG
XM_011544097.1:c.361+73_361+74delinsGG XP_011542399.1:n.361+73_361+74delinsGG
XM_006711749.3:c.361+73_361+74delinsGG XP_006711812.1:n.361+73_361+74delinsGG
XM_017000394.1:c.484+73_484+74delinsGG XP_016855883.1:n.484+73_484+74delinsGG
XM_017000395.1:c.484+73_484+74delinsGG XP_016855884.1:n.484+73_484+74delinsGG
XR_001736987.1:n.649+73_649+74delinsGG
XR_001736988.1:n.649+73_649+74delinsGG
XR_001736989.1:n.649+73_649+74delinsGG
XR_001736990.1:n.532+73_532+74delinsGG
NM_152490.5:c.361+73_361+74delinsGG MANE Select NP_689703.1:n.361+73_361+74delinsGG
NM_001277155.3:c.484+73_484+74delinsGG NP_001264084.1:n.484+73_484+74delinsGG