Canonical Allele Identifier: CA1603684715

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608653_177608662delinsAGCTGCGGTG , CM000667.2:g.177608653_177608662delinsAGCTGCGGTG	GRCh38
NC_000005.9:g.177035654_177035663delinsAGCTGCGGTG , CM000667.1:g.177035654_177035663delinsAGCTGCGGTG	GRCh37
NC_000005.8:g.176968260_176968269delinsAGCTGCGGTG	NCBI36
NG_015977.1:g.13536_13545delinsAGCTGCGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+31_723+40delinsAGCTGCGGTG MANE Select	ENSP00000029410.5:n.723+31_723+40delinsAGCTGCGGTG
ENST00000029410.9:c.723+31_723+40delinsAGCTGCGGTG	ENSP00000029410.5:n.723+31_723+40delinsAGCTGCGGTG
ENST00000505145.1:n.1821+31_1821+40delinsAGCTGCGGTG
ENST00000505433.5:c.*229+31_*229+40delinsAGCTGCGGTG	ENSP00000425591.1:n.*229+31_*229+40delinsAGCTGCGGTG
ENST00000515353.1:n.1289_1298delinsAGCTGCGGTG
NM_007255.2:c.723+31_723+40delinsAGCTGCGGTG	NP_009186.1:n.723+31_723+40delinsAGCTGCGGTG
XM_005265805.2:c.381+31_381+40delinsAGCTGCGGTG	XP_005265862.1:n.381+31_381+40delinsAGCTGCGGTG
XM_006714816.2:c.243+31_243+40delinsAGCTGCGGTG	XP_006714879.1:n.243+31_243+40delinsAGCTGCGGTG
XM_011534421.1:c.381+31_381+40delinsAGCTGCGGTG	XP_011532723.1:n.381+31_381+40delinsAGCTGCGGTG
XM_006714816.4:c.243+31_243+40delinsAGCTGCGGTG	XP_006714879.1:n.243+31_243+40delinsAGCTGCGGTG
XM_017008999.2:c.381+31_381+40delinsAGCTGCGGTG	XP_016864488.1:n.381+31_381+40delinsAGCTGCGGTG
NM_007255.3:c.723+31_723+40delinsAGCTGCGGTG MANE Select	NP_009186.1:n.723+31_723+40delinsAGCTGCGGTG