Canonical Allele Identifier: CA1603730388

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604400_177604403delinsGCCC , CM000667.2:g.177604400_177604403delinsGCCC	GRCh38
NC_000005.9:g.177031401_177031404delinsGCCC , CM000667.1:g.177031401_177031404delinsGCCC	GRCh37
NC_000005.8:g.176964007_176964010delinsGCCC	NCBI36
NG_015977.1:g.9283_9286delinsGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.272_275delinsGCCC MANE Select	ENSP00000029410.5:p.Gly91=
ENST00000029410.9:c.272_275delinsGCCC	ENSP00000029410.5:p.Gly91=
ENST00000502420.1:n.251_254delinsGCCC
ENST00000505433.5:c.272_275delinsGCCC	ENSP00000425591.1:p.Gly91=
ENST00000505468.1:c.-71_-68delinsGCCC	ENSP00000420886.1:n.-71_-68delinsGCCC
ENST00000507061.1:c.89_92delinsGCCC	ENSP00000423868.1:p.Gly30=
ENST00000510761.1:c.-71_-68delinsGCCC	ENSP00000423438.1:n.-71_-68delinsGCCC
NM_007255.2:c.272_275delinsGCCC	NP_009186.1:p.Gly91=
XM_005265805.2:c.-71_-68delinsGCCC	XP_005265862.1:n.-71_-68delinsGCCC
XM_006714816.2:c.-228_-225delinsGCCC	XP_006714879.1:n.-228_-225delinsGCCC
XM_011534421.1:c.-71_-68delinsGCCC	XP_011532723.1:n.-71_-68delinsGCCC
XM_006714816.4:c.-228_-225delinsGCCC	XP_006714879.1:n.-228_-225delinsGCCC
XM_017008999.2:c.-71_-68delinsGCCC	XP_016864488.1:n.-71_-68delinsGCCC
NM_007255.3:c.272_275delinsGCCC MANE Select	NP_009186.1:p.Gly91=