Canonical Allele Identifier: CA2326044650
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816764C= , CM000681.2:g.17816764C= GRCh38
NC_000019.9:g.17927573C= , CM000681.1:g.17927573C= GRCh37
NC_000019.8:g.17788573C= NCBI36
NG_012092.1:g.9748G=

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.*90G= MANE Select ENSP00000321724.6:n.*90G=
ENST00000317306.7:c.*90G= ENSP00000321724.6:n.*90G=
ENST00000379695.5:c.*107G= ENSP00000369017.4:n.*107G=
ENST00000598577.1:c.507G=
NM_001265587.1:c.*107G= NP_001252516.1:n.*107G=
NM_005543.3:c.*90G= NP_005534.2:n.*90G=
NM_001265587.2:c.*107G= NP_001252516.1:n.*107G=
NM_005543.4:c.*90G= MANE Select NP_005534.2:n.*90G=