Canonical Allele Identifier: CA404760821
Gene: INSL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816960G>A , CM000681.2:g.17816960G>A GRCh38
NC_000019.9:g.17927769G>A , CM000681.1:g.17927769G>A GRCh37
NC_000019.8:g.17788769G>A NCBI36
NG_012092.1:g.9552C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.290C>T MANE Select ENSP00000321724.6:p.Thr97Ile
ENST00000317306.7:c.290C>T ENSP00000321724.6:p.Thr97Ile
ENST00000379695.5:c.385C>T ENSP00000369017.4:p.Pro129Ser
ENST00000598577.1:c.311C>T
NM_001265587.1:c.385C>T NP_001252516.1:p.Pro129Ser
NM_005543.3:c.290C>T NP_005534.2:p.Thr97Ile
NM_001265587.2:c.385C>T NP_001252516.1:p.Pro129Ser
NM_005543.4:c.290C>T MANE Select NP_005534.2:p.Thr97Ile