Canonical Allele Identifier: CA447985294

Gene: B4GALT7

Linked Data

• MyVariant Identifiers: chr5:g.177035928A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608927A>C , CM000667.2:g.177608927A>C	GRCh38
NC_000005.9:g.177035928A>C , CM000667.1:g.177035928A>C	GRCh37
NC_000005.8:g.176968534A>C	NCBI36
NG_015977.1:g.13810A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.741A>C MANE Select	ENSP00000029410.5:p.Gly247=
ENST00000029410.9:c.741A>C	ENSP00000029410.5:p.Gly247=
ENST00000505145.1:n.1839A>C
ENST00000505433.5:c.*247A>C	ENSP00000425591.1:n.*247A>C
ENST00000515353.1:n.1563A>C
NM_007255.2:c.741A>C	NP_009186.1:p.Gly247=
XM_005265805.2:c.399A>C	XP_005265862.1:p.Gly133=
XM_006714816.2:c.261A>C	XP_006714879.1:p.Gly87=
XM_011534421.1:c.399A>C	XP_011532723.1:p.Gly133=
XM_006714816.4:c.261A>C	XP_006714879.1:p.Gly87=
XM_017008999.2:c.399A>C	XP_016864488.1:p.Gly133=
NM_007255.3:c.741A>C MANE Select	NP_009186.1:p.Gly247=