Canonical Allele Identifier: CA1603685893

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609131_177609132delinsAG , CM000667.2:g.177609131_177609132delinsAG	GRCh38
NC_000005.9:g.177036132_177036133delinsAG , CM000667.1:g.177036132_177036133delinsAG	GRCh37
NC_000005.8:g.176968738_176968739delinsAG	NCBI36
NG_015977.1:g.14014_14015delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+117_828+118delinsAG MANE Select	ENSP00000029410.5:n.828+117_828+118delinsAG
ENST00000029410.9:c.828+117_828+118delinsAG	ENSP00000029410.5:n.828+117_828+118delinsAG
ENST00000505145.1:n.1926+117_1926+118delinsAG
ENST00000505433.5:c.*334+117_*334+118delinsAG	ENSP00000425591.1:n.*334+117_*334+118delinsAG
ENST00000515353.1:n.1650+117_1650+118delinsAG
NM_007255.2:c.828+117_828+118delinsAG	NP_009186.1:n.828+117_828+118delinsAG
XM_005265805.2:c.486+117_486+118delinsAG	XP_005265862.1:n.486+117_486+118delinsAG
XM_006714816.2:c.348+117_348+118delinsAG	XP_006714879.1:n.348+117_348+118delinsAG
XM_011534421.1:c.486+117_486+118delinsAG	XP_011532723.1:n.486+117_486+118delinsAG
XM_006714816.4:c.348+117_348+118delinsAG	XP_006714879.1:n.348+117_348+118delinsAG
XM_017008999.2:c.486+117_486+118delinsAG	XP_016864488.1:n.486+117_486+118delinsAG
NM_007255.3:c.828+117_828+118delinsAG MANE Select	NP_009186.1:n.828+117_828+118delinsAG