Canonical Allele Identifier: CA2326044658
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816779C= , CM000681.2:g.17816779C= GRCh38
NC_000019.9:g.17927588C= , CM000681.1:g.17927588C= GRCh37
NC_000019.8:g.17788588C= NCBI36
NG_012092.1:g.9733G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*75G= MANE Select ENSP00000321724.6:n.*75G=
ENST00000317306.7:c.*75G= ENSP00000321724.6:n.*75G=
ENST00000379695.5:c.*92G= ENSP00000369017.4:n.*92G=
ENST00000598577.1:c.492G=
NM_001265587.1:c.*92G= NP_001252516.1:n.*92G=
NM_005543.3:c.*75G= NP_005534.2:n.*75G=
NM_001265587.2:c.*92G= NP_001252516.1:n.*92G=
NM_005543.4:c.*75G= MANE Select NP_005534.2:n.*75G=