Canonical Allele Identifier: CA1603684969

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608793_177608796delinsTCTC , CM000667.2:g.177608793_177608796delinsTCTC	GRCh38
NC_000005.9:g.177035794_177035797delinsTCTC , CM000667.1:g.177035794_177035797delinsTCTC	GRCh37
NC_000005.8:g.176968400_176968403delinsTCTC	NCBI36
NG_015977.1:g.13676_13679delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-117_724-114delinsTCTC MANE Select	ENSP00000029410.5:n.724-117_724-114delinsTCTC
ENST00000029410.9:c.724-117_724-114delinsTCTC	ENSP00000029410.5:n.724-117_724-114delinsTCTC
ENST00000505145.1:n.1822-117_1822-114delinsTCTC
ENST00000505433.5:c.*230-117_*230-114delinsTCTC	ENSP00000425591.1:n.*230-117_*230-114delinsTCTC
ENST00000515353.1:n.1429_1432delinsTCTC
NM_007255.2:c.724-117_724-114delinsTCTC	NP_009186.1:n.724-117_724-114delinsTCTC
XM_005265805.2:c.382-117_382-114delinsTCTC	XP_005265862.1:n.382-117_382-114delinsTCTC
XM_006714816.2:c.244-117_244-114delinsTCTC	XP_006714879.1:n.244-117_244-114delinsTCTC
XM_011534421.1:c.382-117_382-114delinsTCTC	XP_011532723.1:n.382-117_382-114delinsTCTC
XM_006714816.4:c.244-117_244-114delinsTCTC	XP_006714879.1:n.244-117_244-114delinsTCTC
XM_017008999.2:c.382-117_382-114delinsTCTC	XP_016864488.1:n.382-117_382-114delinsTCTC
NM_007255.3:c.724-117_724-114delinsTCTC MANE Select	NP_009186.1:n.724-117_724-114delinsTCTC