Canonical Allele Identifier: CA2326045295
Gene: INSL3 HGNC NCBI

Linked Data

dbSNP Id: rs10421916
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17818178A>T , CM000681.2:g.17818178A>T GRCh38
NC_000019.9:g.17928987A>T , CM000681.1:g.17928987A>T GRCh37
NC_000019.8:g.17789987A>T NCBI36
NG_012092.1:g.8334T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.191-1119T>A MANE Select ENSP00000321724.6:n.191-1119T>A
ENST00000317306.7:c.191-1119T>A ENSP00000321724.6:n.191-1119T>A
ENST00000379695.5:c.286-1119T>A ENSP00000369017.4:n.286-1119T>A
ENST00000598577.1:c.190-1097T>A
NM_001265587.1:c.286-1119T>A NP_001252516.1:n.286-1119T>A
NM_005543.3:c.191-1119T>A NP_005534.2:n.191-1119T>A
NM_001265587.2:c.286-1119T>A NP_001252516.1:n.286-1119T>A
NM_005543.4:c.191-1119T>A MANE Select NP_005534.2:n.191-1119T>A
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