Canonical Allele Identifier: CA1603684851

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608721_177608723delinsCCT , CM000667.2:g.177608721_177608723delinsCCT	GRCh38
NC_000005.9:g.177035722_177035724delinsCCT , CM000667.1:g.177035722_177035724delinsCCT	GRCh37
NC_000005.8:g.176968328_176968330delinsCCT	NCBI36
NG_015977.1:g.13604_13606delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+99_723+101delinsCCT MANE Select	ENSP00000029410.5:n.723+99_723+101delinsCCT
ENST00000029410.9:c.723+99_723+101delinsCCT	ENSP00000029410.5:n.723+99_723+101delinsCCT
ENST00000505145.1:n.1821+99_1821+101delinsCCT
ENST00000505433.5:c.*229+99_*229+101delinsCCT	ENSP00000425591.1:n.*229+99_*229+101delinsCCT
ENST00000515353.1:n.1357_1359delinsCCT
NM_007255.2:c.723+99_723+101delinsCCT	NP_009186.1:n.723+99_723+101delinsCCT
XM_005265805.2:c.381+99_381+101delinsCCT	XP_005265862.1:n.381+99_381+101delinsCCT
XM_006714816.2:c.243+99_243+101delinsCCT	XP_006714879.1:n.243+99_243+101delinsCCT
XM_011534421.1:c.381+99_381+101delinsCCT	XP_011532723.1:n.381+99_381+101delinsCCT
XM_006714816.4:c.243+99_243+101delinsCCT	XP_006714879.1:n.243+99_243+101delinsCCT
XM_017008999.2:c.381+99_381+101delinsCCT	XP_016864488.1:n.381+99_381+101delinsCCT
NM_007255.3:c.723+99_723+101delinsCCT MANE Select	NP_009186.1:n.723+99_723+101delinsCCT