Canonical Allele Identifier: CA404760797
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816952G>A , CM000681.2:g.17816952G>A GRCh38
NC_000019.9:g.17927761G>A , CM000681.1:g.17927761G>A GRCh37
NC_000019.8:g.17788761G>A NCBI36
NG_012092.1:g.9560C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.298C>T MANE Select ENSP00000321724.6:p.His100Tyr
ENST00000317306.7:c.298C>T ENSP00000321724.6:p.His100Tyr
ENST00000379695.5:c.393C>T ENSP00000369017.4:p.Thr131=
ENST00000598577.1:c.319C>T
NM_001265587.1:c.393C>T NP_001252516.1:p.Thr131=
NM_005543.3:c.298C>T NP_005534.2:p.His100Tyr
NM_001265587.2:c.393C>T NP_001252516.1:p.Thr131=
NM_005543.4:c.298C>T MANE Select NP_005534.2:p.His100Tyr