Canonical Allele Identifier: CA1603685110

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608873_177608874delinsAG , CM000667.2:g.177608873_177608874delinsAG	GRCh38
NC_000005.9:g.177035874_177035875delinsAG , CM000667.1:g.177035874_177035875delinsAG	GRCh37
NC_000005.8:g.176968480_176968481delinsAG	NCBI36
NG_015977.1:g.13756_13757delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-37_724-36delinsAG MANE Select	ENSP00000029410.5:n.724-37_724-36delinsAG
ENST00000029410.9:c.724-37_724-36delinsAG	ENSP00000029410.5:n.724-37_724-36delinsAG
ENST00000505145.1:n.1822-37_1822-36delinsAG
ENST00000505433.5:c.*230-37_*230-36delinsAG	ENSP00000425591.1:n.*230-37_*230-36delinsAG
ENST00000515353.1:n.1509_1510delinsAG
NM_007255.2:c.724-37_724-36delinsAG	NP_009186.1:n.724-37_724-36delinsAG
XM_005265805.2:c.382-37_382-36delinsAG	XP_005265862.1:n.382-37_382-36delinsAG
XM_006714816.2:c.244-37_244-36delinsAG	XP_006714879.1:n.244-37_244-36delinsAG
XM_011534421.1:c.382-37_382-36delinsAG	XP_011532723.1:n.382-37_382-36delinsAG
XM_006714816.4:c.244-37_244-36delinsAG	XP_006714879.1:n.244-37_244-36delinsAG
XM_017008999.2:c.382-37_382-36delinsAG	XP_016864488.1:n.382-37_382-36delinsAG
NM_007255.3:c.724-37_724-36delinsAG MANE Select	NP_009186.1:n.724-37_724-36delinsAG