Canonical Allele Identifier: CA2676759897

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177609138-TCGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609141_177609143del , CM000667.2:g.177609141_177609143del	GRCh38
NC_000005.9:g.177036142_177036144del , CM000667.1:g.177036142_177036144del	GRCh37
NC_000005.8:g.176968748_176968750del	NCBI36
NG_015977.1:g.14024_14026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+127_828+129del MANE Select	ENSP00000029410.5:n.828+127_828+129del
ENST00000029410.9:c.828+127_828+129del	ENSP00000029410.5:n.828+127_828+129del
ENST00000505145.1:n.1926+127_1926+129del
ENST00000505433.5:c.*334+127_*334+129del	ENSP00000425591.1:n.*334+127_*334+129del
ENST00000515353.1:n.1650+127_1650+129del
NM_007255.2:c.828+127_828+129del	NP_009186.1:n.828+127_828+129del
XM_005265805.2:c.486+127_486+129del	XP_005265862.1:n.486+127_486+129del
XM_006714816.2:c.348+127_348+129del	XP_006714879.1:n.348+127_348+129del
XM_011534421.1:c.486+127_486+129del	XP_011532723.1:n.486+127_486+129del
XM_006714816.4:c.348+127_348+129del	XP_006714879.1:n.348+127_348+129del
XM_017008999.2:c.486+127_486+129del	XP_016864488.1:n.486+127_486+129del
NM_007255.3:c.828+127_828+129del MANE Select	NP_009186.1:n.828+127_828+129del