Canonical Allele Identifier: CA1700793162

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906653A= , CM000669.2:g.37906653A= GRCh38
NC_000007.13:g.37946255A= , CM000669.1:g.37946255A= GRCh37
NC_000007.12:g.37912780A= NCBI36
NG_052980.1:g.15271T=

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*826T= (SFRP4) MANE Select ENSP00000410715.2:n.*826T=
ENST00000436072.6:c.*826T= (SFRP4) ENSP00000410715.2:n.*826T=
ENST00000476620.1:c.-37-42187A= (EPDR1) ENSP00000425858.1:n.-37-42187A=
NM_003014.3:c.*826T= (SFRP4) NP_003005.2:n.*826T=
NM_003014.4:c.*826T= (SFRP4) MANE Select NP_003005.2:n.*826T=