Canonical Allele Identifier: CA1603684790

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608674_177608689delinsATTTTCTTCTGTTTCC , CM000667.2:g.177608674_177608689delinsATTTTCTTCTGTTTCC	GRCh38
NC_000005.9:g.177035675_177035690delinsATTTTCTTCTGTTTCC , CM000667.1:g.177035675_177035690delinsATTTTCTTCTGTTTCC	GRCh37
NC_000005.8:g.176968281_176968296delinsATTTTCTTCTGTTTCC	NCBI36
NG_015977.1:g.13557_13572delinsATTTTCTTCTGTTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+52_723+67delinsATTTTCTTCTGTTTCC MANE Select	ENSP00000029410.5:n.723+52_723+67delinsATTTTCTTCTGTTTCC
ENST00000029410.9:c.723+52_723+67delinsATTTTCTTCTGTTTCC	ENSP00000029410.5:n.723+52_723+67delinsATTTTCTTCTGTTTCC
ENST00000505145.1:n.1821+52_1821+67delinsATTTTCTTCTGTTTCC
ENST00000505433.5:c.*229+52_*229+67delinsATTTTCTTCTGTTTCC	ENSP00000425591.1:n.*229+52_*229+67delinsATTTTCTTCTGTTTCC
ENST00000515353.1:n.1310_1325delinsATTTTCTTCTGTTTCC
NM_007255.2:c.723+52_723+67delinsATTTTCTTCTGTTTCC	NP_009186.1:n.723+52_723+67delinsATTTTCTTCTGTTTCC
XM_005265805.2:c.381+52_381+67delinsATTTTCTTCTGTTTCC	XP_005265862.1:n.381+52_381+67delinsATTTTCTTCTGTTTCC
XM_006714816.2:c.243+52_243+67delinsATTTTCTTCTGTTTCC	XP_006714879.1:n.243+52_243+67delinsATTTTCTTCTGTTTCC
XM_011534421.1:c.381+52_381+67delinsATTTTCTTCTGTTTCC	XP_011532723.1:n.381+52_381+67delinsATTTTCTTCTGTTTCC
XM_006714816.4:c.243+52_243+67delinsATTTTCTTCTGTTTCC	XP_006714879.1:n.243+52_243+67delinsATTTTCTTCTGTTTCC
XM_017008999.2:c.381+52_381+67delinsATTTTCTTCTGTTTCC	XP_016864488.1:n.381+52_381+67delinsATTTTCTTCTGTTTCC
NM_007255.3:c.723+52_723+67delinsATTTTCTTCTGTTTCC MANE Select	NP_009186.1:n.723+52_723+67delinsATTTTCTTCTGTTTCC