Canonical Allele Identifier: CA404760792
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816950A>G , CM000681.2:g.17816950A>G GRCh38
NC_000019.9:g.17927759A>G , CM000681.1:g.17927759A>G GRCh37
NC_000019.8:g.17788759A>G NCBI36
NG_012092.1:g.9562T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.300T>C MANE Select ENSP00000321724.6:p.His100=
ENST00000317306.7:c.300T>C ENSP00000321724.6:p.His100=
ENST00000379695.5:c.395T>C ENSP00000369017.4:p.Ile132Thr
ENST00000598577.1:c.321T>C
NM_001265587.1:c.395T>C NP_001252516.1:p.Ile132Thr
NM_005543.3:c.300T>C NP_005534.2:p.His100=
NM_001265587.2:c.395T>C NP_001252516.1:p.Ile132Thr
NM_005543.4:c.300T>C MANE Select NP_005534.2:p.His100=