Canonical Allele Identifier: CA1700793134

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906563_37906564delinsAT , CM000669.2:g.37906563_37906564delinsAT GRCh38
NC_000007.13:g.37946165_37946166delinsAT , CM000669.1:g.37946165_37946166delinsAT GRCh37
NC_000007.12:g.37912690_37912691delinsAT NCBI36
NG_052980.1:g.15360_15361delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000436072.7:c.*915_*916delinsAT (SFRP4) MANE Select ENSP00000410715.2:n.*915_*916delinsAT
ENST00000436072.6:c.*915_*916delinsAT (SFRP4) ENSP00000410715.2:n.*915_*916delinsAT
ENST00000476620.1:c.-37-42277_-37-42276delinsAT (EPDR1) ENSP00000425858.1:n.-37-42277_-37-42276delinsAT
NM_003014.3:c.*915_*916delinsAT (SFRP4) NP_003005.2:n.*915_*916delinsAT
NM_003014.4:c.*915_*916delinsAT (SFRP4) MANE Select NP_003005.2:n.*915_*916delinsAT