Canonical Allele Identifier: CA1778879942
Gene: SFRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262205G= , CM000670.2:g.41262205G= GRCh38
NC_000008.10:g.41119724G= , CM000670.1:g.41119724G= GRCh37
NC_000008.9:g.41238881G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2962C= MANE Select ENSP00000220772.3:n.*2962C=
ENST00000220772.7:c.*2962C= ENSP00000220772.3:n.*2962C=
ENST00000379845.3:c.*2962C= ENSP00000369174.3:n.*2962C=
NM_003012.4:c.*2962C= NP_003003.3:n.*2962C=
NM_003012.5:c.*2962C= MANE Select NP_003003.3:n.*2962C=