Canonical Allele Identifier: CA447984253

Gene: B4GALT7

Linked Data

• MyVariant Identifiers: chr5:g.177031417A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604416A>T , CM000667.2:g.177604416A>T	GRCh38
NC_000005.9:g.177031417A>T , CM000667.1:g.177031417A>T	GRCh37
NC_000005.8:g.176964023A>T	NCBI36
NG_015977.1:g.9299A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.288A>T MANE Select	ENSP00000029410.5:p.Ala96=
ENST00000029410.9:c.288A>T	ENSP00000029410.5:p.Ala96=
ENST00000502420.1:n.267A>T
ENST00000505433.5:c.288A>T	ENSP00000425591.1:p.Ala96=
ENST00000505468.1:c.-55A>T	ENSP00000420886.1:n.-55A>T
ENST00000507061.1:c.105A>T	ENSP00000423868.1:p.Ala35=
ENST00000510761.1:c.-55A>T	ENSP00000423438.1:n.-55A>T
NM_007255.2:c.288A>T	NP_009186.1:p.Ala96=
XM_005265805.2:c.-55A>T	XP_005265862.1:n.-55A>T
XM_006714816.2:c.-212A>T	XP_006714879.1:n.-212A>T
XM_011534421.1:c.-55A>T	XP_011532723.1:n.-55A>T
XM_006714816.4:c.-212A>T	XP_006714879.1:n.-212A>T
XM_017008999.2:c.-55A>T	XP_016864488.1:n.-55A>T
NM_007255.3:c.288A>T MANE Select	NP_009186.1:p.Ala96=