Canonical Allele Identifier: CA404760786
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816948T>A , CM000681.2:g.17816948T>A GRCh38
NC_000019.9:g.17927757T>A , CM000681.1:g.17927757T>A GRCh37
NC_000019.8:g.17788757T>A NCBI36
NG_012092.1:g.9564A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.302A>T MANE Select ENSP00000321724.6:p.His101Leu
ENST00000317306.7:c.302A>T ENSP00000321724.6:p.His101Leu
ENST00000379695.5:c.397A>T ENSP00000369017.4:p.Thr133Ser
ENST00000598577.1:c.323A>T
NM_001265587.1:c.397A>T NP_001252516.1:p.Thr133Ser
NM_005543.3:c.302A>T NP_005534.2:p.His101Leu
NM_001265587.2:c.397A>T NP_001252516.1:p.Thr133Ser
NM_005543.4:c.302A>T MANE Select NP_005534.2:p.His101Leu