Canonical Allele Identifier: CA404760606
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816882T>C , CM000681.2:g.17816882T>C GRCh38
NC_000019.9:g.17927691T>C , CM000681.1:g.17927691T>C GRCh37
NC_000019.8:g.17788691T>C NCBI36
NG_012092.1:g.9630A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.368A>G MANE Select ENSP00000321724.6:p.Gln123Arg
ENST00000317306.7:c.368A>G ENSP00000321724.6:p.Gln123Arg
ENST00000379695.5:c.463A>G ENSP00000369017.4:p.Lys155Glu
ENST00000598577.1:c.389A>G
NM_001265587.1:c.463A>G NP_001252516.1:p.Lys155Glu
NM_005543.3:c.368A>G NP_005534.2:p.Gln123Arg
NM_001265587.2:c.463A>G NP_001252516.1:p.Lys155Glu
NM_005543.4:c.368A>G MANE Select NP_005534.2:p.Gln123Arg