Canonical Allele Identifier: CA1603684674

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608634_177608635delinsCG , CM000667.2:g.177608634_177608635delinsCG	GRCh38
NC_000005.9:g.177035635_177035636delinsCG , CM000667.1:g.177035635_177035636delinsCG	GRCh37
NC_000005.8:g.176968241_176968242delinsCG	NCBI36
NG_015977.1:g.13517_13518delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+12_723+13delinsCG MANE Select	ENSP00000029410.5:n.723+12_723+13delinsCG
ENST00000029410.9:c.723+12_723+13delinsCG	ENSP00000029410.5:n.723+12_723+13delinsCG
ENST00000505145.1:n.1821+12_1821+13delinsCG
ENST00000505433.5:c.*229+12_*229+13delinsCG	ENSP00000425591.1:n.*229+12_*229+13delinsCG
ENST00000515353.1:n.1270_1271delinsCG
NM_007255.2:c.723+12_723+13delinsCG	NP_009186.1:n.723+12_723+13delinsCG
XM_005265805.2:c.381+12_381+13delinsCG	XP_005265862.1:n.381+12_381+13delinsCG
XM_006714816.2:c.243+12_243+13delinsCG	XP_006714879.1:n.243+12_243+13delinsCG
XM_011534421.1:c.381+12_381+13delinsCG	XP_011532723.1:n.381+12_381+13delinsCG
XM_006714816.4:c.243+12_243+13delinsCG	XP_006714879.1:n.243+12_243+13delinsCG
XM_017008999.2:c.381+12_381+13delinsCG	XP_016864488.1:n.381+12_381+13delinsCG
NM_007255.3:c.723+12_723+13delinsCG MANE Select	NP_009186.1:n.723+12_723+13delinsCG