Canonical Allele Identifier: CA2682437929

Linked Data

gnomAD v4: 7-37906902-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906902T>G , CM000669.2:g.37906902T>G GRCh38
NC_000007.13:g.37946504T>G , CM000669.1:g.37946504T>G GRCh37
NC_000007.12:g.37913029T>G NCBI36
NG_052980.1:g.15022A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000436072.7:c.*577A>C (SFRP4) MANE Select ENSP00000410715.2:n.*577A>C
ENST00000436072.6:c.*577A>C (SFRP4) ENSP00000410715.2:n.*577A>C
ENST00000476620.1:c.-37-41938T>G (EPDR1) ENSP00000425858.1:n.-37-41938T>G
NM_003014.3:c.*577A>C (SFRP4) NP_003005.2:n.*577A>C
NM_003014.4:c.*577A>C (SFRP4) MANE Select NP_003005.2:n.*577A>C