Canonical Allele Identifier: CA1778880001
Gene: SFRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262335A= , CM000670.2:g.41262335A= GRCh38
NC_000008.10:g.41119854A= , CM000670.1:g.41119854A= GRCh37
NC_000008.9:g.41239011A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2832T= MANE Select ENSP00000220772.3:n.*2832T=
ENST00000220772.7:c.*2832T= ENSP00000220772.3:n.*2832T=
ENST00000379845.3:c.*2832T= ENSP00000369174.3:n.*2832T=
NM_003012.4:c.*2832T= NP_003003.3:n.*2832T=
NM_003012.5:c.*2832T= MANE Select NP_003003.3:n.*2832T=