Canonical Allele Identifier: CA2326044660
Gene: INSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816784T= , CM000681.2:g.17816784T= GRCh38
NC_000019.9:g.17927593T= , CM000681.1:g.17927593T= GRCh37
NC_000019.8:g.17788593T= NCBI36
NG_012092.1:g.9728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*70A= MANE Select ENSP00000321724.6:n.*70A=
ENST00000317306.7:c.*70A= ENSP00000321724.6:n.*70A=
ENST00000379695.5:c.*87A= ENSP00000369017.4:n.*87A=
ENST00000598577.1:c.487A=
NM_001265587.1:c.*87A= NP_001252516.1:n.*87A=
NM_005543.3:c.*70A= NP_005534.2:n.*70A=
NM_001265587.2:c.*87A= NP_001252516.1:n.*87A=
NM_005543.4:c.*70A= MANE Select NP_005534.2:n.*70A=