Canonical Allele Identifier: CA1603685737

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609033_177609034delinsAT , CM000667.2:g.177609033_177609034delinsAT	GRCh38
NC_000005.9:g.177036034_177036035delinsAT , CM000667.1:g.177036034_177036035delinsAT	GRCh37
NC_000005.8:g.176968640_176968641delinsAT	NCBI36
NG_015977.1:g.13916_13917delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+19_828+20delinsAT MANE Select	ENSP00000029410.5:n.828+19_828+20delinsAT
ENST00000029410.9:c.828+19_828+20delinsAT	ENSP00000029410.5:n.828+19_828+20delinsAT
ENST00000505145.1:n.1926+19_1926+20delinsAT
ENST00000505433.5:c.*334+19_*334+20delinsAT	ENSP00000425591.1:n.*334+19_*334+20delinsAT
ENST00000515353.1:n.1650+19_1650+20delinsAT
NM_007255.2:c.828+19_828+20delinsAT	NP_009186.1:n.828+19_828+20delinsAT
XM_005265805.2:c.486+19_486+20delinsAT	XP_005265862.1:n.486+19_486+20delinsAT
XM_006714816.2:c.348+19_348+20delinsAT	XP_006714879.1:n.348+19_348+20delinsAT
XM_011534421.1:c.486+19_486+20delinsAT	XP_011532723.1:n.486+19_486+20delinsAT
XM_006714816.4:c.348+19_348+20delinsAT	XP_006714879.1:n.348+19_348+20delinsAT
XM_017008999.2:c.486+19_486+20delinsAT	XP_016864488.1:n.486+19_486+20delinsAT
NM_007255.3:c.828+19_828+20delinsAT MANE Select	NP_009186.1:n.828+19_828+20delinsAT