Canonical Allele Identifier: CA1603684939

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608785_177608787delinsGGC , CM000667.2:g.177608785_177608787delinsGGC	GRCh38
NC_000005.9:g.177035786_177035788delinsGGC , CM000667.1:g.177035786_177035788delinsGGC	GRCh37
NC_000005.8:g.176968392_176968394delinsGGC	NCBI36
NG_015977.1:g.13668_13670delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-125_724-123delinsGGC MANE Select	ENSP00000029410.5:n.724-125_724-123delinsGGC
ENST00000029410.9:c.724-125_724-123delinsGGC	ENSP00000029410.5:n.724-125_724-123delinsGGC
ENST00000505145.1:n.1822-125_1822-123delinsGGC
ENST00000505433.5:c.*230-125_*230-123delinsGGC	ENSP00000425591.1:n.*230-125_*230-123delinsGGC
ENST00000515353.1:n.1421_1423delinsGGC
NM_007255.2:c.724-125_724-123delinsGGC	NP_009186.1:n.724-125_724-123delinsGGC
XM_005265805.2:c.382-125_382-123delinsGGC	XP_005265862.1:n.382-125_382-123delinsGGC
XM_006714816.2:c.244-125_244-123delinsGGC	XP_006714879.1:n.244-125_244-123delinsGGC
XM_011534421.1:c.382-125_382-123delinsGGC	XP_011532723.1:n.382-125_382-123delinsGGC
XM_006714816.4:c.244-125_244-123delinsGGC	XP_006714879.1:n.244-125_244-123delinsGGC
XM_017008999.2:c.382-125_382-123delinsGGC	XP_016864488.1:n.382-125_382-123delinsGGC
NM_007255.3:c.724-125_724-123delinsGGC MANE Select	NP_009186.1:n.724-125_724-123delinsGGC