Canonical Allele Identifier: CA2516682949

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906686del , CM000669.2:g.37906686del GRCh38
NC_000007.13:g.37946288del , CM000669.1:g.37946288del GRCh37
NC_000007.12:g.37912813del NCBI36
NG_052980.1:g.15239del

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*794del (SFRP4) MANE Select ENSP00000410715.2:n.*794del
ENST00000436072.6:c.*794del (SFRP4) ENSP00000410715.2:n.*794del
ENST00000476620.1:c.-37-42154del (EPDR1) ENSP00000425858.1:n.-37-42154del
NM_003014.3:c.*794del (SFRP4) NP_003005.2:n.*794del
NM_003014.4:c.*794del (SFRP4) MANE Select NP_003005.2:n.*794del