Canonical Allele Identifier: CA1603730216

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604118_177604119delinsCG , CM000667.2:g.177604118_177604119delinsCG	GRCh38
NC_000005.9:g.177031119_177031120delinsCG , CM000667.1:g.177031119_177031120delinsCG	GRCh37
NC_000005.8:g.176963725_176963726delinsCG	NCBI36
NG_015977.1:g.9001_9002delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.51-61_51-60delinsCG MANE Select	ENSP00000029410.5:n.51-61_51-60delinsCG
ENST00000029410.9:c.51-61_51-60delinsCG	ENSP00000029410.5:n.51-61_51-60delinsCG
ENST00000502420.1:n.130-161_130-160delinsCG
ENST00000505433.5:c.51-61_51-60delinsCG	ENSP00000425591.1:n.51-61_51-60delinsCG
ENST00000505468.1:c.-353_-352delinsCG	ENSP00000420886.1:n.-353_-352delinsCG
ENST00000510761.1:c.-292-61_-292-60delinsCG	ENSP00000423438.1:n.-292-61_-292-60delinsCG
NM_007255.2:c.51-61_51-60delinsCG	NP_009186.1:n.51-61_51-60delinsCG
XM_005265805.2:c.-292-61_-292-60delinsCG	XP_005265862.1:n.-292-61_-292-60delinsCG
XM_006714816.2:c.-449-61_-449-60delinsCG	XP_006714879.1:n.-449-61_-449-60delinsCG
XM_011534421.1:c.-292-61_-292-60delinsCG	XP_011532723.1:n.-292-61_-292-60delinsCG
XM_006714816.4:c.-449-61_-449-60delinsCG	XP_006714879.1:n.-449-61_-449-60delinsCG
XM_017008999.2:c.-292-61_-292-60delinsCG	XP_016864488.1:n.-292-61_-292-60delinsCG
NM_007255.3:c.51-61_51-60delinsCG MANE Select	NP_009186.1:n.51-61_51-60delinsCG