Canonical Allele Identifier: CA1700793207

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906781C= , CM000669.2:g.37906781C= GRCh38
NC_000007.13:g.37946383C= , CM000669.1:g.37946383C= GRCh37
NC_000007.12:g.37912908C= NCBI36
NG_052980.1:g.15143G=

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*698G= (SFRP4) MANE Select ENSP00000410715.2:n.*698G=
ENST00000436072.6:c.*698G= (SFRP4) ENSP00000410715.2:n.*698G=
ENST00000476620.1:c.-37-42059C= (EPDR1) ENSP00000425858.1:n.-37-42059C=
NM_003014.3:c.*698G= (SFRP4) NP_003005.2:n.*698G=
NM_003014.4:c.*698G= (SFRP4) MANE Select NP_003005.2:n.*698G=