Canonical Allele Identifier: CA404760809
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816956A>C , CM000681.2:g.17816956A>C GRCh38
NC_000019.9:g.17927765A>C , CM000681.1:g.17927765A>C GRCh37
NC_000019.8:g.17788765A>C NCBI36
NG_012092.1:g.9556T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.294T>G MANE Select ENSP00000321724.6:p.Ser98=
ENST00000317306.7:c.294T>G ENSP00000321724.6:p.Ser98=
ENST00000379695.5:c.389T>G ENSP00000369017.4:p.Leu130Arg
ENST00000598577.1:c.315T>G
NM_001265587.1:c.389T>G NP_001252516.1:p.Leu130Arg
NM_005543.3:c.294T>G NP_005534.2:p.Ser98=
NM_001265587.2:c.389T>G NP_001252516.1:p.Leu130Arg
NM_005543.4:c.294T>G MANE Select NP_005534.2:p.Ser98=