Canonical Allele Identifier: CA404760617
Gene: INSL3 HGNC NCBI

Linked Data

COSMIC: COSM3388723
MyVariant Identifiers: chr19:g.17927695G>T (hg19) chr19:g.17816886G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816886G>T , CM000681.2:g.17816886G>T GRCh38
NC_000019.9:g.17927695G>T , CM000681.1:g.17927695G>T GRCh37
NC_000019.8:g.17788695G>T NCBI36
NG_012092.1:g.9626C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.364C>A MANE Select ENSP00000321724.6:p.Gln122Lys
ENST00000317306.7:c.364C>A ENSP00000321724.6:p.Gln122Lys
ENST00000379695.5:c.459C>A ENSP00000369017.4:p.Pro153=
ENST00000598577.1:c.385C>A
NM_001265587.1:c.459C>A NP_001252516.1:p.Pro153=
NM_005543.3:c.364C>A NP_005534.2:p.Gln122Lys
NM_001265587.2:c.459C>A NP_001252516.1:p.Pro153=
NM_005543.4:c.364C>A MANE Select NP_005534.2:p.Gln122Lys
Search 100 bp 5'
Search 100 bp 3'