Canonical Allele Identifier: CA2326044646
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816761A= , CM000681.2:g.17816761A= GRCh38
NC_000019.9:g.17927570A= , CM000681.1:g.17927570A= GRCh37
NC_000019.8:g.17788570A= NCBI36
NG_012092.1:g.9751T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*93T= MANE Select ENSP00000321724.6:n.*93T=
ENST00000317306.7:c.*93T= ENSP00000321724.6:n.*93T=
ENST00000379695.5:c.*110T= ENSP00000369017.4:n.*110T=
ENST00000598577.1:c.510T=
NM_001265587.1:c.*110T= NP_001252516.1:n.*110T=
NM_005543.3:c.*93T= NP_005534.2:n.*93T=
NM_001265587.2:c.*110T= NP_001252516.1:n.*110T=
NM_005543.4:c.*93T= MANE Select NP_005534.2:n.*93T=