Canonical Allele Identifier: CA1778879952
Gene: SFRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262226T= , CM000670.2:g.41262226T= GRCh38
NC_000008.10:g.41119745T= , CM000670.1:g.41119745T= GRCh37
NC_000008.9:g.41238902T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2941A= MANE Select ENSP00000220772.3:n.*2941A=
ENST00000220772.7:c.*2941A= ENSP00000220772.3:n.*2941A=
ENST00000379845.3:c.*2941A= ENSP00000369174.3:n.*2941A=
NM_003012.4:c.*2941A= NP_003003.3:n.*2941A=
NM_003012.5:c.*2941A= MANE Select NP_003003.3:n.*2941A=