Canonical Allele Identifier: CA2326044663
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816800C= , CM000681.2:g.17816800C= GRCh38
NC_000019.9:g.17927609C= , CM000681.1:g.17927609C= GRCh37
NC_000019.8:g.17788609C= NCBI36
NG_012092.1:g.9712G=

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.*54G= MANE Select ENSP00000321724.6:n.*54G=
ENST00000317306.7:c.*54G= ENSP00000321724.6:n.*54G=
ENST00000379695.5:c.*71G= ENSP00000369017.4:n.*71G=
ENST00000598577.1:c.471G=
NM_001265587.1:c.*71G= NP_001252516.1:n.*71G=
NM_005543.3:c.*54G= NP_005534.2:n.*54G=
NM_001265587.2:c.*71G= NP_001252516.1:n.*71G=
NM_005543.4:c.*54G= MANE Select NP_005534.2:n.*54G=