Canonical Allele Identifier: CA2486521345

Gene: B3GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235489037_235489039delinsAAG , CM000663.2:g.235489037_235489039delinsAAG	GRCh38
NC_000001.10:g.235652342_235652344delinsAAG , CM000663.1:g.235652342_235652344delinsAAG	GRCh37
NC_000001.9:g.233718965_233718967delinsAAG	NCBI36
NG_033219.2:g.20443_20445delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.361+129_361+131delinsCTT MANE Select	ENSP00000355559.3:n.361+129_361+131delinsCTT
ENST00000675193.1:c.484+129_484+131delinsCTT	ENSP00000502069.1:n.484+129_484+131delinsCTT
ENST00000675555.1:c.139+129_139+131delinsCTT	ENSP00000501896.1:n.139+129_139+131delinsCTT
ENST00000676288.1:c.484+129_484+131delinsCTT	ENSP00000502392.1:n.484+129_484+131delinsCTT
ENST00000313984.3:c.484+129_484+131delinsCTT	ENSP00000315678.3:n.484+129_484+131delinsCTT
ENST00000366600.7:c.361+129_361+131delinsCTT	ENSP00000355559.3:n.361+129_361+131delinsCTT
ENST00000494378.1:n.434-4524_434-4522delinsCTT
ENST00000612859.4:c.261-4524_261-4522delinsCTT	ENSP00000481548.1:n.261-4524_261-4522delinsCTT
NM_001277155.2:c.484+129_484+131delinsCTT	NP_001264084.1:n.484+129_484+131delinsCTT
NM_152490.4:c.361+129_361+131delinsCTT	NP_689703.1:n.361+129_361+131delinsCTT
XM_005273071.3:c.361+129_361+131delinsCTT	XP_005273128.1:n.361+129_361+131delinsCTT
XM_006711749.2:c.361+129_361+131delinsCTT	XP_006711812.1:n.361+129_361+131delinsCTT
XM_011544096.1:c.361+129_361+131delinsCTT	XP_011542398.1:n.361+129_361+131delinsCTT
XM_011544097.1:c.361+129_361+131delinsCTT	XP_011542399.1:n.361+129_361+131delinsCTT
XM_006711749.3:c.361+129_361+131delinsCTT	XP_006711812.1:n.361+129_361+131delinsCTT
XM_017000394.1:c.484+129_484+131delinsCTT	XP_016855883.1:n.484+129_484+131delinsCTT
XM_017000395.1:c.484+129_484+131delinsCTT	XP_016855884.1:n.484+129_484+131delinsCTT
XR_001736987.1:n.649+129_649+131delinsCTT
XR_001736988.1:n.649+129_649+131delinsCTT
XR_001736989.1:n.649+129_649+131delinsCTT
XR_001736990.1:n.532+129_532+131delinsCTT
NM_152490.5:c.361+129_361+131delinsCTT MANE Select	NP_689703.1:n.361+129_361+131delinsCTT
NM_001277155.3:c.484+129_484+131delinsCTT	NP_001264084.1:n.484+129_484+131delinsCTT