Canonical Allele Identifier: CA1603730383

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604395_177604396delinsCT , CM000667.2:g.177604395_177604396delinsCT	GRCh38
NC_000005.9:g.177031396_177031397delinsCT , CM000667.1:g.177031396_177031397delinsCT	GRCh37
NC_000005.8:g.176964002_176964003delinsCT	NCBI36
NG_015977.1:g.9278_9279delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000029410.10:c.267_268delinsCT MANE Select	ENSP00000029410.5:p.Ser89=
ENST00000029410.9:c.267_268delinsCT	ENSP00000029410.5:p.Ser89=
ENST00000502420.1:n.246_247delinsCT
ENST00000505433.5:c.267_268delinsCT	ENSP00000425591.1:p.Ser89=
ENST00000505468.1:c.-76_-75delinsCT	ENSP00000420886.1:n.-76_-75delinsCT
ENST00000507061.1:c.84_85delinsCT	ENSP00000423868.1:p.Ser28=
ENST00000510761.1:c.-76_-75delinsCT	ENSP00000423438.1:n.-76_-75delinsCT
NM_007255.2:c.267_268delinsCT	NP_009186.1:p.Ser89=
XM_005265805.2:c.-76_-75delinsCT	XP_005265862.1:n.-76_-75delinsCT
XM_006714816.2:c.-233_-232delinsCT	XP_006714879.1:n.-233_-232delinsCT
XM_011534421.1:c.-76_-75delinsCT	XP_011532723.1:n.-76_-75delinsCT
XM_006714816.4:c.-233_-232delinsCT	XP_006714879.1:n.-233_-232delinsCT
XM_017008999.2:c.-76_-75delinsCT	XP_016864488.1:n.-76_-75delinsCT
NM_007255.3:c.267_268delinsCT MANE Select	NP_009186.1:p.Ser89=