Canonical Allele Identifier: CA2326044648
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816763G= , CM000681.2:g.17816763G= GRCh38
NC_000019.9:g.17927572G= , CM000681.1:g.17927572G= GRCh37
NC_000019.8:g.17788572G= NCBI36
NG_012092.1:g.9749C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*91C= MANE Select ENSP00000321724.6:n.*91C=
ENST00000317306.7:c.*91C= ENSP00000321724.6:n.*91C=
ENST00000379695.5:c.*108C= ENSP00000369017.4:n.*108C=
ENST00000598577.1:c.508C=
NM_001265587.1:c.*108C= NP_001252516.1:n.*108C=
NM_005543.3:c.*91C= NP_005534.2:n.*91C=
NM_001265587.2:c.*108C= NP_001252516.1:n.*108C=
NM_005543.4:c.*91C= MANE Select NP_005534.2:n.*91C=