Canonical Allele Identifier: CA506002139
Gene: INSL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17927686G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816877G>A , CM000681.2:g.17816877G>A GRCh38
NC_000019.9:g.17927686G>A , CM000681.1:g.17927686G>A GRCh37
NC_000019.8:g.17788686G>A NCBI36
NG_012092.1:g.9635C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.373C>T MANE Select ENSP00000321724.6:p.Leu125=
ENST00000317306.7:c.373C>T ENSP00000321724.6:p.Leu125=
ENST00000379695.5:c.468C>T ENSP00000369017.4:p.Thr156=
ENST00000598577.1:c.394C>T
NM_001265587.1:c.468C>T NP_001252516.1:p.Thr156=
NM_005543.3:c.373C>T NP_005534.2:p.Leu125=
NM_001265587.2:c.468C>T NP_001252516.1:p.Thr156=
NM_005543.4:c.373C>T MANE Select NP_005534.2:p.Leu125=