Canonical Allele Identifier: CA404760812
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816957G>T , CM000681.2:g.17816957G>T GRCh38
NC_000019.9:g.17927766G>T , CM000681.1:g.17927766G>T GRCh37
NC_000019.8:g.17788766G>T NCBI36
NG_012092.1:g.9555C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.293C>A MANE Select ENSP00000321724.6:p.Ser98Tyr
ENST00000317306.7:c.293C>A ENSP00000321724.6:p.Ser98Tyr
ENST00000379695.5:c.388C>A ENSP00000369017.4:p.Leu130Ile
ENST00000598577.1:c.314C>A
NM_001265587.1:c.388C>A NP_001252516.1:p.Leu130Ile
NM_005543.3:c.293C>A NP_005534.2:p.Ser98Tyr
NM_001265587.2:c.388C>A NP_001252516.1:p.Leu130Ile
NM_005543.4:c.293C>A MANE Select NP_005534.2:p.Ser98Tyr