Canonical Allele Identifier: CA1700793205

Linked Data

dbSNP Id: rs1785401871

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906780dup , CM000669.2:g.37906780dup GRCh38
NC_000007.13:g.37946382dup , CM000669.1:g.37946382dup GRCh37
NC_000007.12:g.37912907dup NCBI36
NG_052980.1:g.15149dup

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*704dup (SFRP4) MANE Select ENSP00000410715.2:n.*704dup
ENST00000436072.6:c.*704dup (SFRP4) ENSP00000410715.2:n.*704dup
ENST00000476620.1:c.-37-42060dup (EPDR1) ENSP00000425858.1:n.-37-42060dup
NM_003014.3:c.*704dup (SFRP4) NP_003005.2:n.*704dup
NM_003014.4:c.*704dup (SFRP4) MANE Select NP_003005.2:n.*704dup