Canonical Allele Identifier: CA1603730389

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604400_177604405delinsGCCCCC , CM000667.2:g.177604400_177604405delinsGCCCCC	GRCh38
NC_000005.9:g.177031401_177031406delinsGCCCCC , CM000667.1:g.177031401_177031406delinsGCCCCC	GRCh37
NC_000005.8:g.176964007_176964012delinsGCCCCC	NCBI36
NG_015977.1:g.9283_9288delinsGCCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000029410.10:c.272_277delinsGCCCCC MANE Select	ENSP00000029410.5:p.Gly91=
ENST00000029410.9:c.272_277delinsGCCCCC	ENSP00000029410.5:p.Gly91=
ENST00000502420.1:n.251_256delinsGCCCCC
ENST00000505433.5:c.272_277delinsGCCCCC	ENSP00000425591.1:p.Gly91=
ENST00000505468.1:c.-71_-66delinsGCCCCC	ENSP00000420886.1:n.-71_-66delinsGCCCCC
ENST00000507061.1:c.89_94delinsGCCCCC	ENSP00000423868.1:p.Gly30=
ENST00000510761.1:c.-71_-66delinsGCCCCC	ENSP00000423438.1:n.-71_-66delinsGCCCCC
NM_007255.2:c.272_277delinsGCCCCC	NP_009186.1:p.Gly91=
XM_005265805.2:c.-71_-66delinsGCCCCC	XP_005265862.1:n.-71_-66delinsGCCCCC
XM_006714816.2:c.-228_-223delinsGCCCCC	XP_006714879.1:n.-228_-223delinsGCCCCC
XM_011534421.1:c.-71_-66delinsGCCCCC	XP_011532723.1:n.-71_-66delinsGCCCCC
XM_006714816.4:c.-228_-223delinsGCCCCC	XP_006714879.1:n.-228_-223delinsGCCCCC
XM_017008999.2:c.-71_-66delinsGCCCCC	XP_016864488.1:n.-71_-66delinsGCCCCC
NM_007255.3:c.272_277delinsGCCCCC MANE Select	NP_009186.1:p.Gly91=