Canonical Allele Identifier: CA1113098619
Gene: SFRP1 HGNC NCBI

Linked Data

dbSNP Id: rs1803385584

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262354dup , CM000670.2:g.41262354dup GRCh38
NC_000008.10:g.41119873dup , CM000670.1:g.41119873dup GRCh37
NC_000008.9:g.41239030dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2813dup MANE Select ENSP00000220772.3:n.*2813dup
ENST00000220772.7:c.*2813dup ENSP00000220772.3:n.*2813dup
ENST00000379845.3:c.*2813dup ENSP00000369174.3:n.*2813dup
NM_003012.4:c.*2813dup NP_003003.3:n.*2813dup
NM_003012.5:c.*2813dup MANE Select NP_003003.3:n.*2813dup