Canonical Allele Identifier: CA132897038

Gene: B4GALT7

Linked Data

• dbSNP Id: rs997538045
• gnomAD v3: 5-177609132-GGTCA-G
• gnomAD v4: 5-177609132-GGTCA-G
• MyVariant Identifiers: chr5:g.177036134_177036137del (hg19) ; chr5:g.177609133_177609136del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609136_177609139del , CM000667.2:g.177609136_177609139del	GRCh38
NC_000005.9:g.177036137_177036140del , CM000667.1:g.177036137_177036140del	GRCh37
NC_000005.8:g.176968743_176968746del	NCBI36
NG_015977.1:g.14019_14022del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+122_828+125del MANE Select	ENSP00000029410.5:n.828+122_828+125del
ENST00000029410.9:c.828+122_828+125del	ENSP00000029410.5:n.828+122_828+125del
ENST00000505145.1:n.1926+122_1926+125del
ENST00000505433.5:c.*334+122_*334+125del	ENSP00000425591.1:n.*334+122_*334+125del
ENST00000515353.1:n.1650+122_1650+125del
NM_007255.2:c.828+122_828+125del	NP_009186.1:n.828+122_828+125del
XM_005265805.2:c.486+122_486+125del	XP_005265862.1:n.486+122_486+125del
XM_006714816.2:c.348+122_348+125del	XP_006714879.1:n.348+122_348+125del
XM_011534421.1:c.486+122_486+125del	XP_011532723.1:n.486+122_486+125del
XM_006714816.4:c.348+122_348+125del	XP_006714879.1:n.348+122_348+125del
XM_017008999.2:c.486+122_486+125del	XP_016864488.1:n.486+122_486+125del
NM_007255.3:c.828+122_828+125del MANE Select	NP_009186.1:n.828+122_828+125del