Canonical Allele Identifier: CA2583418999
Gene: INSL3 HGNC NCBI

Linked Data

gnomAD v4: 19-17816794-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816794A>T , CM000681.2:g.17816794A>T GRCh38
NC_000019.9:g.17927603A>T , CM000681.1:g.17927603A>T GRCh37
NC_000019.8:g.17788603A>T NCBI36
NG_012092.1:g.9718T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317306.8:c.*60T>A MANE Select ENSP00000321724.6:n.*60T>A
ENST00000317306.7:c.*60T>A ENSP00000321724.6:n.*60T>A
ENST00000379695.5:c.*77T>A ENSP00000369017.4:n.*77T>A
ENST00000598577.1:c.477T>A
NM_001265587.1:c.*77T>A NP_001252516.1:n.*77T>A
NM_005543.3:c.*60T>A NP_005534.2:n.*60T>A
NM_001265587.2:c.*77T>A NP_001252516.1:n.*77T>A
NM_005543.4:c.*60T>A MANE Select NP_005534.2:n.*60T>A
Search 100 bp 5'
Search 100 bp 3'