Canonical Allele Identifier: CA2326044657
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816778G= , CM000681.2:g.17816778G= GRCh38
NC_000019.9:g.17927587G= , CM000681.1:g.17927587G= GRCh37
NC_000019.8:g.17788587G= NCBI36
NG_012092.1:g.9734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*76C= MANE Select ENSP00000321724.6:n.*76C=
ENST00000317306.7:c.*76C= ENSP00000321724.6:n.*76C=
ENST00000379695.5:c.*93C= ENSP00000369017.4:n.*93C=
ENST00000598577.1:c.493C=
NM_001265587.1:c.*93C= NP_001252516.1:n.*93C=
NM_005543.3:c.*76C= NP_005534.2:n.*76C=
NM_001265587.2:c.*93C= NP_001252516.1:n.*93C=
NM_005543.4:c.*76C= MANE Select NP_005534.2:n.*76C=