Canonical Allele Identifier: CA1603685767

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609062_177609064delinsAGC , CM000667.2:g.177609062_177609064delinsAGC	GRCh38
NC_000005.9:g.177036063_177036065delinsAGC , CM000667.1:g.177036063_177036065delinsAGC	GRCh37
NC_000005.8:g.176968669_176968671delinsAGC	NCBI36
NG_015977.1:g.13945_13947delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+48_828+50delinsAGC MANE Select	ENSP00000029410.5:n.828+48_828+50delinsAGC
ENST00000029410.9:c.828+48_828+50delinsAGC	ENSP00000029410.5:n.828+48_828+50delinsAGC
ENST00000505145.1:n.1926+48_1926+50delinsAGC
ENST00000505433.5:c.*334+48_*334+50delinsAGC	ENSP00000425591.1:n.*334+48_*334+50delinsAGC
ENST00000515353.1:n.1650+48_1650+50delinsAGC
NM_007255.2:c.828+48_828+50delinsAGC	NP_009186.1:n.828+48_828+50delinsAGC
XM_005265805.2:c.486+48_486+50delinsAGC	XP_005265862.1:n.486+48_486+50delinsAGC
XM_006714816.2:c.348+48_348+50delinsAGC	XP_006714879.1:n.348+48_348+50delinsAGC
XM_011534421.1:c.486+48_486+50delinsAGC	XP_011532723.1:n.486+48_486+50delinsAGC
XM_006714816.4:c.348+48_348+50delinsAGC	XP_006714879.1:n.348+48_348+50delinsAGC
XM_017008999.2:c.486+48_486+50delinsAGC	XP_016864488.1:n.486+48_486+50delinsAGC
NM_007255.3:c.828+48_828+50delinsAGC MANE Select	NP_009186.1:n.828+48_828+50delinsAGC