Canonical Allele Identifier: CA2769582039

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609110_177609111del , CM000667.2:g.177609110_177609111del	GRCh38
NC_000005.9:g.177036111_177036112del , CM000667.1:g.177036111_177036112del	GRCh37
NC_000005.8:g.176968717_176968718del	NCBI36
NG_015977.1:g.13993_13994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+96_828+97del MANE Select	ENSP00000029410.5:n.828+96_828+97del
ENST00000029410.9:c.828+96_828+97del	ENSP00000029410.5:n.828+96_828+97del
ENST00000505145.1:n.1926+96_1926+97del
ENST00000505433.5:c.*334+96_*334+97del	ENSP00000425591.1:n.*334+96_*334+97del
ENST00000515353.1:n.1650+96_1650+97del
NM_007255.2:c.828+96_828+97del	NP_009186.1:n.828+96_828+97del
XM_005265805.2:c.486+96_486+97del	XP_005265862.1:n.486+96_486+97del
XM_006714816.2:c.348+96_348+97del	XP_006714879.1:n.348+96_348+97del
XM_011534421.1:c.486+96_486+97del	XP_011532723.1:n.486+96_486+97del
XM_006714816.4:c.348+96_348+97del	XP_006714879.1:n.348+96_348+97del
XM_017008999.2:c.486+96_486+97del	XP_016864488.1:n.486+96_486+97del
NM_007255.3:c.828+96_828+97del MANE Select	NP_009186.1:n.828+96_828+97del