Canonical Allele Identifier: CA1603684678

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608637_177608638delinsGC , CM000667.2:g.177608637_177608638delinsGC	GRCh38
NC_000005.9:g.177035638_177035639delinsGC , CM000667.1:g.177035638_177035639delinsGC	GRCh37
NC_000005.8:g.176968244_176968245delinsGC	NCBI36
NG_015977.1:g.13520_13521delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+15_723+16delinsGC MANE Select	ENSP00000029410.5:n.723+15_723+16delinsGC
ENST00000029410.9:c.723+15_723+16delinsGC	ENSP00000029410.5:n.723+15_723+16delinsGC
ENST00000505145.1:n.1821+15_1821+16delinsGC
ENST00000505433.5:c.*229+15_*229+16delinsGC	ENSP00000425591.1:n.*229+15_*229+16delinsGC
ENST00000515353.1:n.1273_1274delinsGC
NM_007255.2:c.723+15_723+16delinsGC	NP_009186.1:n.723+15_723+16delinsGC
XM_005265805.2:c.381+15_381+16delinsGC	XP_005265862.1:n.381+15_381+16delinsGC
XM_006714816.2:c.243+15_243+16delinsGC	XP_006714879.1:n.243+15_243+16delinsGC
XM_011534421.1:c.381+15_381+16delinsGC	XP_011532723.1:n.381+15_381+16delinsGC
XM_006714816.4:c.243+15_243+16delinsGC	XP_006714879.1:n.243+15_243+16delinsGC
XM_017008999.2:c.381+15_381+16delinsGC	XP_016864488.1:n.381+15_381+16delinsGC
NM_007255.3:c.723+15_723+16delinsGC MANE Select	NP_009186.1:n.723+15_723+16delinsGC