Canonical Allele Identifier: CA1603685909

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609138_177609143delinsTCGACG , CM000667.2:g.177609138_177609143delinsTCGACG	GRCh38
NC_000005.9:g.177036139_177036144delinsTCGACG , CM000667.1:g.177036139_177036144delinsTCGACG	GRCh37
NC_000005.8:g.176968745_176968750delinsTCGACG	NCBI36
NG_015977.1:g.14021_14026delinsTCGACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+124_828+129delinsTCGACG MANE Select	ENSP00000029410.5:n.828+124_828+129delinsTCGACG
ENST00000029410.9:c.828+124_828+129delinsTCGACG	ENSP00000029410.5:n.828+124_828+129delinsTCGACG
ENST00000505145.1:n.1926+124_1926+129delinsTCGACG
ENST00000505433.5:c.*334+124_*334+129delinsTCGACG	ENSP00000425591.1:n.*334+124_*334+129delinsTCGACG
ENST00000515353.1:n.1650+124_1650+129delinsTCGACG
NM_007255.2:c.828+124_828+129delinsTCGACG	NP_009186.1:n.828+124_828+129delinsTCGACG
XM_005265805.2:c.486+124_486+129delinsTCGACG	XP_005265862.1:n.486+124_486+129delinsTCGACG
XM_006714816.2:c.348+124_348+129delinsTCGACG	XP_006714879.1:n.348+124_348+129delinsTCGACG
XM_011534421.1:c.486+124_486+129delinsTCGACG	XP_011532723.1:n.486+124_486+129delinsTCGACG
XM_006714816.4:c.348+124_348+129delinsTCGACG	XP_006714879.1:n.348+124_348+129delinsTCGACG
XM_017008999.2:c.486+124_486+129delinsTCGACG	XP_016864488.1:n.486+124_486+129delinsTCGACG
NM_007255.3:c.828+124_828+129delinsTCGACG MANE Select	NP_009186.1:n.828+124_828+129delinsTCGACG