Canonical Allele Identifier: CA2326044652
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816766A= , CM000681.2:g.17816766A= GRCh38
NC_000019.9:g.17927575A= , CM000681.1:g.17927575A= GRCh37
NC_000019.8:g.17788575A= NCBI36
NG_012092.1:g.9746T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*88T= MANE Select ENSP00000321724.6:n.*88T=
ENST00000317306.7:c.*88T= ENSP00000321724.6:n.*88T=
ENST00000379695.5:c.*105T= ENSP00000369017.4:n.*105T=
ENST00000598577.1:c.505T=
NM_001265587.1:c.*105T= NP_001252516.1:n.*105T=
NM_005543.3:c.*88T= NP_005534.2:n.*88T=
NM_001265587.2:c.*105T= NP_001252516.1:n.*105T=
NM_005543.4:c.*88T= MANE Select NP_005534.2:n.*88T=