Canonical Allele Identifier: CA1603684932

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608781_177608782delinsTG , CM000667.2:g.177608781_177608782delinsTG	GRCh38
NC_000005.9:g.177035782_177035783delinsTG , CM000667.1:g.177035782_177035783delinsTG	GRCh37
NC_000005.8:g.176968388_176968389delinsTG	NCBI36
NG_015977.1:g.13664_13665delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-129_724-128delinsTG MANE Select	ENSP00000029410.5:n.724-129_724-128delinsTG
ENST00000029410.9:c.724-129_724-128delinsTG	ENSP00000029410.5:n.724-129_724-128delinsTG
ENST00000505145.1:n.1822-129_1822-128delinsTG
ENST00000505433.5:c.*230-129_*230-128delinsTG	ENSP00000425591.1:n.*230-129_*230-128delinsTG
ENST00000515353.1:n.1417_1418delinsTG
NM_007255.2:c.724-129_724-128delinsTG	NP_009186.1:n.724-129_724-128delinsTG
XM_005265805.2:c.382-129_382-128delinsTG	XP_005265862.1:n.382-129_382-128delinsTG
XM_006714816.2:c.244-129_244-128delinsTG	XP_006714879.1:n.244-129_244-128delinsTG
XM_011534421.1:c.382-129_382-128delinsTG	XP_011532723.1:n.382-129_382-128delinsTG
XM_006714816.4:c.244-129_244-128delinsTG	XP_006714879.1:n.244-129_244-128delinsTG
XM_017008999.2:c.382-129_382-128delinsTG	XP_016864488.1:n.382-129_382-128delinsTG
NM_007255.3:c.724-129_724-128delinsTG MANE Select	NP_009186.1:n.724-129_724-128delinsTG