Canonical Allele Identifier: CA1100334638

Linked Data

gnomAD v3: 7-37906774-C-A
gnomAD v4: 7-37906774-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906774C>A , CM000669.2:g.37906774C>A GRCh38
NC_000007.13:g.37946376C>A , CM000669.1:g.37946376C>A GRCh37
NC_000007.12:g.37912901C>A NCBI36
NG_052980.1:g.15150G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*705G>T (SFRP4) MANE Select ENSP00000410715.2:n.*705G>T
ENST00000436072.6:c.*705G>T (SFRP4) ENSP00000410715.2:n.*705G>T
ENST00000476620.1:c.-37-42066C>A (EPDR1) ENSP00000425858.1:n.-37-42066C>A
NM_003014.3:c.*705G>T (SFRP4) NP_003005.2:n.*705G>T
NM_003014.4:c.*705G>T (SFRP4) MANE Select NP_003005.2:n.*705G>T