Canonical Allele Identifier: CA1603685992

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609166C= , CM000667.2:g.177609166C=	GRCh38
NC_000005.9:g.177036167C= , CM000667.1:g.177036167C=	GRCh37
NC_000005.8:g.176968773C=	NCBI36
NG_015977.1:g.14049C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+152C= MANE Select	ENSP00000029410.5:n.828+152C=
ENST00000029410.9:c.828+152C=	ENSP00000029410.5:n.828+152C=
ENST00000505145.1:n.1926+152C=
ENST00000505433.5:c.*334+152C=	ENSP00000425591.1:n.*334+152C=
ENST00000515353.1:n.1650+152C=
NM_007255.2:c.828+152C=	NP_009186.1:n.828+152C=
XM_005265805.2:c.486+152C=	XP_005265862.1:n.486+152C=
XM_006714816.2:c.348+152C=	XP_006714879.1:n.348+152C=
XM_011534421.1:c.486+152C=	XP_011532723.1:n.486+152C=
XM_006714816.4:c.348+152C=	XP_006714879.1:n.348+152C=
XM_017008999.2:c.486+152C=	XP_016864488.1:n.486+152C=
NM_007255.3:c.828+152C= MANE Select	NP_009186.1:n.828+152C=