Canonical Allele Identifier: CA1700793182

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906708T= , CM000669.2:g.37906708T= GRCh38
NC_000007.13:g.37946310T= , CM000669.1:g.37946310T= GRCh37
NC_000007.12:g.37912835T= NCBI36
NG_052980.1:g.15216A=

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*771A= (SFRP4) MANE Select ENSP00000410715.2:n.*771A=
ENST00000436072.6:c.*771A= (SFRP4) ENSP00000410715.2:n.*771A=
ENST00000476620.1:c.-37-42132T= (EPDR1) ENSP00000425858.1:n.-37-42132T=
NM_003014.3:c.*771A= (SFRP4) NP_003005.2:n.*771A=
NM_003014.4:c.*771A= (SFRP4) MANE Select NP_003005.2:n.*771A=