Canonical Allele Identifier: CA1603686039

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609195_177609196delinsTG , CM000667.2:g.177609195_177609196delinsTG	GRCh38
NC_000005.9:g.177036196_177036197delinsTG , CM000667.1:g.177036196_177036197delinsTG	GRCh37
NC_000005.8:g.176968802_176968803delinsTG	NCBI36
NG_015977.1:g.14078_14079delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+181_828+182delinsTG MANE Select	ENSP00000029410.5:n.828+181_828+182delinsTG
ENST00000029410.9:c.828+181_828+182delinsTG	ENSP00000029410.5:n.828+181_828+182delinsTG
ENST00000505145.1:n.1926+181_1926+182delinsTG
ENST00000505433.5:c.*334+181_*334+182delinsTG	ENSP00000425591.1:n.*334+181_*334+182delinsTG
ENST00000515353.1:n.1650+181_1650+182delinsTG
NM_007255.2:c.828+181_828+182delinsTG	NP_009186.1:n.828+181_828+182delinsTG
XM_005265805.2:c.486+181_486+182delinsTG	XP_005265862.1:n.486+181_486+182delinsTG
XM_006714816.2:c.348+181_348+182delinsTG	XP_006714879.1:n.348+181_348+182delinsTG
XM_011534421.1:c.486+181_486+182delinsTG	XP_011532723.1:n.486+181_486+182delinsTG
XM_006714816.4:c.348+181_348+182delinsTG	XP_006714879.1:n.348+181_348+182delinsTG
XM_017008999.2:c.486+181_486+182delinsTG	XP_016864488.1:n.486+181_486+182delinsTG
NM_007255.3:c.828+181_828+182delinsTG MANE Select	NP_009186.1:n.828+181_828+182delinsTG