Canonical Allele Identifier: CA404760576
Gene: INSL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17927679G>T (hg19) chr19:g.17816870G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816870G>T , CM000681.2:g.17816870G>T GRCh38
NC_000019.9:g.17927679G>T , CM000681.1:g.17927679G>T GRCh37
NC_000019.8:g.17788679G>T NCBI36
NG_012092.1:g.9642C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.380C>A MANE Select ENSP00000321724.6:p.Thr127Asn
ENST00000317306.7:c.380C>A ENSP00000321724.6:p.Thr127Asn
ENST00000379695.5:c.*1C>A ENSP00000369017.4:n.*1C>A
ENST00000598577.1:c.401C>A
NM_001265587.1:c.*1C>A NP_001252516.1:n.*1C>A
NM_005543.3:c.380C>A NP_005534.2:p.Thr127Asn
NM_001265587.2:c.*1C>A NP_001252516.1:n.*1C>A
NM_005543.4:c.380C>A MANE Select NP_005534.2:p.Thr127Asn
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