Canonical Allele Identifier: CA651603484

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906553_37906554insA , CM000669.2:g.37906553_37906554insA GRCh38
NC_000007.13:g.37946155_37946156insA , CM000669.1:g.37946155_37946156insA GRCh37
NC_000007.12:g.37912680_37912681insA NCBI36
NG_052980.1:g.15370_15371insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000436072.7:c.*925_*926insT (SFRP4) MANE Select ENSP00000410715.2:n.*925_*926insT
ENST00000436072.6:c.*925_*926insT (SFRP4) ENSP00000410715.2:n.*925_*926insT
ENST00000476620.1:c.-37-42287_-37-42286insA (EPDR1) ENSP00000425858.1:n.-37-42287_-37-42286insA
NM_003014.3:c.*925_*926insT (SFRP4) NP_003005.2:n.*925_*926insT
NM_003014.4:c.*925_*926insT (SFRP4) MANE Select NP_003005.2:n.*925_*926insT