Canonical Allele Identifier: CA1603730291

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604246_177604249delinsTCGC , CM000667.2:g.177604246_177604249delinsTCGC	GRCh38
NC_000005.9:g.177031247_177031250delinsTCGC , CM000667.1:g.177031247_177031250delinsTCGC	GRCh37
NC_000005.8:g.176963853_176963856delinsTCGC	NCBI36
NG_015977.1:g.9129_9132delinsTCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.118_121delinsTCGC MANE Select	ENSP00000029410.5:p.Ser40=
ENST00000029410.9:c.118_121delinsTCGC	ENSP00000029410.5:p.Ser40=
ENST00000502420.1:n.130-33_130-30delinsTCGC
ENST00000505433.5:c.118_121delinsTCGC	ENSP00000425591.1:p.Ser40=
ENST00000505468.1:c.-225_-222delinsTCGC	ENSP00000420886.1:n.-225_-222delinsTCGC
ENST00000510761.1:c.-225_-222delinsTCGC	ENSP00000423438.1:n.-225_-222delinsTCGC
NM_007255.2:c.118_121delinsTCGC	NP_009186.1:p.Ser40=
XM_005265805.2:c.-225_-222delinsTCGC	XP_005265862.1:n.-225_-222delinsTCGC
XM_006714816.2:c.-382_-379delinsTCGC	XP_006714879.1:n.-382_-379delinsTCGC
XM_011534421.1:c.-225_-222delinsTCGC	XP_011532723.1:n.-225_-222delinsTCGC
XM_006714816.4:c.-382_-379delinsTCGC	XP_006714879.1:n.-382_-379delinsTCGC
XM_017008999.2:c.-225_-222delinsTCGC	XP_016864488.1:n.-225_-222delinsTCGC
NM_007255.3:c.118_121delinsTCGC MANE Select	NP_009186.1:p.Ser40=