Canonical Allele Identifier: CA1603686017

Gene: B4GALT7

Linked Data

• dbSNP Id: rs1768105734

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609189_177609190del , CM000667.2:g.177609189_177609190del	GRCh38
NC_000005.9:g.177036190_177036191del , CM000667.1:g.177036190_177036191del	GRCh37
NC_000005.8:g.176968796_176968797del	NCBI36
NG_015977.1:g.14072_14073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+175_828+176del MANE Select	ENSP00000029410.5:n.828+175_828+176del
ENST00000029410.9:c.828+175_828+176del	ENSP00000029410.5:n.828+175_828+176del
ENST00000505145.1:n.1926+175_1926+176del
ENST00000505433.5:c.*334+175_*334+176del	ENSP00000425591.1:n.*334+175_*334+176del
ENST00000515353.1:n.1650+175_1650+176del
NM_007255.2:c.828+175_828+176del	NP_009186.1:n.828+175_828+176del
XM_005265805.2:c.486+175_486+176del	XP_005265862.1:n.486+175_486+176del
XM_006714816.2:c.348+175_348+176del	XP_006714879.1:n.348+175_348+176del
XM_011534421.1:c.486+175_486+176del	XP_011532723.1:n.486+175_486+176del
XM_006714816.4:c.348+175_348+176del	XP_006714879.1:n.348+175_348+176del
XM_017008999.2:c.486+175_486+176del	XP_016864488.1:n.486+175_486+176del
NM_007255.3:c.828+175_828+176del MANE Select	NP_009186.1:n.828+175_828+176del