Canonical Allele Identifier: CA2326044659
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816780T= , CM000681.2:g.17816780T= GRCh38
NC_000019.9:g.17927589T= , CM000681.1:g.17927589T= GRCh37
NC_000019.8:g.17788589T= NCBI36
NG_012092.1:g.9732A=

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.*74A= MANE Select ENSP00000321724.6:n.*74A=
ENST00000317306.7:c.*74A= ENSP00000321724.6:n.*74A=
ENST00000379695.5:c.*91A= ENSP00000369017.4:n.*91A=
ENST00000598577.1:c.491A=
NM_001265587.1:c.*91A= NP_001252516.1:n.*91A=
NM_005543.3:c.*74A= NP_005534.2:n.*74A=
NM_001265587.2:c.*91A= NP_001252516.1:n.*91A=
NM_005543.4:c.*74A= MANE Select NP_005534.2:n.*74A=