Canonical Allele Identifier: CA2326045259
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17818096G= , CM000681.2:g.17818096G= GRCh38
NC_000019.9:g.17928905G= , CM000681.1:g.17928905G= GRCh37
NC_000019.8:g.17789905G= NCBI36
NG_012092.1:g.8416C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.191-1037C= MANE Select ENSP00000321724.6:n.191-1037C=
ENST00000317306.7:c.191-1037C= ENSP00000321724.6:n.191-1037C=
ENST00000379695.5:c.286-1037C= ENSP00000369017.4:n.286-1037C=
ENST00000598577.1:c.190-1015C=
NM_001265587.1:c.286-1037C= NP_001252516.1:n.286-1037C=
NM_005543.3:c.191-1037C= NP_005534.2:n.191-1037C=
NM_001265587.2:c.286-1037C= NP_001252516.1:n.286-1037C=
NM_005543.4:c.191-1037C= MANE Select NP_005534.2:n.191-1037C=