Canonical Allele Identifier: CA2486521322
Gene: B3GALNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235488975_235488976delinsCG , CM000663.2:g.235488975_235488976delinsCG GRCh38
NC_000001.10:g.235652280_235652281delinsCG , CM000663.1:g.235652280_235652281delinsCG GRCh37
NC_000001.9:g.233718903_233718904delinsCG NCBI36
NG_033219.2:g.20506_20507delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366600.8:c.361+192_361+193delinsCG MANE Select ENSP00000355559.3:n.361+192_361+193delinsCG
ENST00000675193.1:c.484+192_484+193delinsCG ENSP00000502069.1:n.484+192_484+193delinsCG
ENST00000675555.1:c.139+192_139+193delinsCG ENSP00000501896.1:n.139+192_139+193delinsCG
ENST00000676288.1:c.484+192_484+193delinsCG ENSP00000502392.1:n.484+192_484+193delinsCG
ENST00000313984.3:c.484+192_484+193delinsCG ENSP00000315678.3:n.484+192_484+193delinsCG
ENST00000366600.7:c.361+192_361+193delinsCG ENSP00000355559.3:n.361+192_361+193delinsCG
ENST00000494378.1:n.434-4461_434-4460delinsCG
ENST00000612859.4:c.261-4461_261-4460delinsCG ENSP00000481548.1:n.261-4461_261-4460delinsCG
NM_001277155.2:c.484+192_484+193delinsCG NP_001264084.1:n.484+192_484+193delinsCG
NM_152490.4:c.361+192_361+193delinsCG NP_689703.1:n.361+192_361+193delinsCG
XM_005273071.3:c.361+192_361+193delinsCG XP_005273128.1:n.361+192_361+193delinsCG
XM_006711749.2:c.361+192_361+193delinsCG XP_006711812.1:n.361+192_361+193delinsCG
XM_011544096.1:c.361+192_361+193delinsCG XP_011542398.1:n.361+192_361+193delinsCG
XM_011544097.1:c.361+192_361+193delinsCG XP_011542399.1:n.361+192_361+193delinsCG
XM_006711749.3:c.361+192_361+193delinsCG XP_006711812.1:n.361+192_361+193delinsCG
XM_017000394.1:c.484+192_484+193delinsCG XP_016855883.1:n.484+192_484+193delinsCG
XM_017000395.1:c.484+192_484+193delinsCG XP_016855884.1:n.484+192_484+193delinsCG
XR_001736987.1:n.649+192_649+193delinsCG
XR_001736988.1:n.649+192_649+193delinsCG
XR_001736989.1:n.649+192_649+193delinsCG
XR_001736990.1:n.532+192_532+193delinsCG
NM_152490.5:c.361+192_361+193delinsCG MANE Select NP_689703.1:n.361+192_361+193delinsCG
NM_001277155.3:c.484+192_484+193delinsCG NP_001264084.1:n.484+192_484+193delinsCG