Canonical Allele Identifier: CA2576716950
Gene: INSL3 HGNC NCBI

Linked Data

gnomAD v4: 19-17816776-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816776G>T , CM000681.2:g.17816776G>T GRCh38
NC_000019.9:g.17927585G>T , CM000681.1:g.17927585G>T GRCh37
NC_000019.8:g.17788585G>T NCBI36
NG_012092.1:g.9736C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.*78C>A MANE Select ENSP00000321724.6:n.*78C>A
ENST00000317306.7:c.*78C>A ENSP00000321724.6:n.*78C>A
ENST00000379695.5:c.*95C>A ENSP00000369017.4:n.*95C>A
ENST00000598577.1:c.495C>A
NM_001265587.1:c.*95C>A NP_001252516.1:n.*95C>A
NM_005543.3:c.*78C>A NP_005534.2:n.*78C>A
NM_001265587.2:c.*95C>A NP_001252516.1:n.*95C>A
NM_005543.4:c.*78C>A MANE Select NP_005534.2:n.*78C>A
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