Canonical Allele Identifier: CA1700793174

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906682_37906686delinsCCTAA , CM000669.2:g.37906682_37906686delinsCCTAA GRCh38
NC_000007.13:g.37946284_37946288delinsCCTAA , CM000669.1:g.37946284_37946288delinsCCTAA GRCh37
NC_000007.12:g.37912809_37912813delinsCCTAA NCBI36
NG_052980.1:g.15238_15242delinsTTAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*793_*797delinsTTAGG (SFRP4) MANE Select ENSP00000410715.2:n.*793_*797delinsTTAGG
ENST00000436072.6:c.*793_*797delinsTTAGG (SFRP4) ENSP00000410715.2:n.*793_*797delinsTTAGG
ENST00000476620.1:c.-37-42158_-37-42154delinsCCTAA (EPDR1) ENSP00000425858.1:n.-37-42158_-37-42154de...
NM_003014.3:c.*793_*797delinsTTAGG (SFRP4) NP_003005.2:n.*793_*797delinsTTAGG
NM_003014.4:c.*793_*797delinsTTAGG (SFRP4) MANE Select NP_003005.2:n.*793_*797delinsTTAGG