Canonical Allele Identifier: CA362376901
Gene: B4GALT7 HGNC NCBI

Linked Data

dbSNP Id: rs1768098034

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177608967C>G , CM000667.2:g.177608967C>G GRCh38
NC_000005.9:g.177035968C>G , CM000667.1:g.177035968C>G GRCh37
NC_000005.8:g.176968574C>G NCBI36
NG_015977.1:g.13850C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000029410.10:c.781C>G MANE Select ENSP00000029410.5:p.Pro261Ala
ENST00000029410.9:c.781C>G ENSP00000029410.5:p.Pro261Ala
ENST00000505145.1:n.1879C>G
ENST00000505433.5:c.*287C>G ENSP00000425591.1:n.*287C>G
ENST00000515353.1:n.1603C>G
NM_007255.2:c.781C>G NP_009186.1:p.Pro261Ala
XM_005265805.2:c.439C>G XP_005265862.1:p.Pro147Ala
XM_006714816.2:c.301C>G XP_006714879.1:p.Pro101Ala
XM_011534421.1:c.439C>G XP_011532723.1:p.Pro147Ala
XM_006714816.4:c.301C>G XP_006714879.1:p.Pro101Ala
XM_017008999.2:c.439C>G XP_016864488.1:p.Pro147Ala
NM_007255.3:c.781C>G MANE Select NP_009186.1:p.Pro261Ala