Canonical Allele Identifier: CA362376791

Gene: B4GALT7

Linked Data

• MyVariant Identifiers: chr5:g.177035947A>T (hg19) ; chr5:g.177608946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608946A>T , CM000667.2:g.177608946A>T	GRCh38
NC_000005.9:g.177035947A>T , CM000667.1:g.177035947A>T	GRCh37
NC_000005.8:g.176968553A>T	NCBI36
NG_015977.1:g.13829A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.760A>T MANE Select	ENSP00000029410.5:p.Thr254Ser
ENST00000029410.9:c.760A>T	ENSP00000029410.5:p.Thr254Ser
ENST00000505145.1:n.1858A>T
ENST00000505433.5:c.*266A>T	ENSP00000425591.1:n.*266A>T
ENST00000515353.1:n.1582A>T
NM_007255.2:c.760A>T	NP_009186.1:p.Thr254Ser
XM_005265805.2:c.418A>T	XP_005265862.1:p.Thr140Ser
XM_006714816.2:c.280A>T	XP_006714879.1:p.Thr94Ser
XM_011534421.1:c.418A>T	XP_011532723.1:p.Thr140Ser
XM_006714816.4:c.280A>T	XP_006714879.1:p.Thr94Ser
XM_017008999.2:c.418A>T	XP_016864488.1:p.Thr140Ser
NM_007255.3:c.760A>T MANE Select	NP_009186.1:p.Thr254Ser