Canonical Allele Identifier: CA2676759628

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177609026-G-GCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609030_177609032dup , CM000667.2:g.177609030_177609032dup	GRCh38
NC_000005.9:g.177036031_177036033dup , CM000667.1:g.177036031_177036033dup	GRCh37
NC_000005.8:g.176968637_176968639dup	NCBI36
NG_015977.1:g.13913_13915dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+16_828+18dup MANE Select	ENSP00000029410.5:n.828+16_828+18dup
ENST00000029410.9:c.828+16_828+18dup	ENSP00000029410.5:n.828+16_828+18dup
ENST00000505145.1:n.1926+16_1926+18dup
ENST00000505433.5:c.*334+16_*334+18dup	ENSP00000425591.1:n.*334+16_*334+18dup
ENST00000515353.1:n.1650+16_1650+18dup
NM_007255.2:c.828+16_828+18dup	NP_009186.1:n.828+16_828+18dup
XM_005265805.2:c.486+16_486+18dup	XP_005265862.1:n.486+16_486+18dup
XM_006714816.2:c.348+16_348+18dup	XP_006714879.1:n.348+16_348+18dup
XM_011534421.1:c.486+16_486+18dup	XP_011532723.1:n.486+16_486+18dup
XM_006714816.4:c.348+16_348+18dup	XP_006714879.1:n.348+16_348+18dup
XM_017008999.2:c.486+16_486+18dup	XP_016864488.1:n.486+16_486+18dup
NM_007255.3:c.828+16_828+18dup MANE Select	NP_009186.1:n.828+16_828+18dup