Canonical Allele Identifier: CA783867405
Gene: INSL3 HGNC NCBI

Linked Data

dbSNP Id: rs1446393680
gnomAD v4: 19-17816773-A-T
MyVariant Identifiers: chr19:g.17927582A>T (hg19) chr19:g.17816773A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816773A>T , CM000681.2:g.17816773A>T GRCh38
NC_000019.9:g.17927582A>T , CM000681.1:g.17927582A>T GRCh37
NC_000019.8:g.17788582A>T NCBI36
NG_012092.1:g.9739T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.*81T>A MANE Select ENSP00000321724.6:n.*81T>A
ENST00000317306.7:c.*81T>A ENSP00000321724.6:n.*81T>A
ENST00000379695.5:c.*98T>A ENSP00000369017.4:n.*98T>A
ENST00000598577.1:c.498T>A
NM_001265587.1:c.*98T>A NP_001252516.1:n.*98T>A
NM_005543.3:c.*81T>A NP_005534.2:n.*81T>A
NM_001265587.2:c.*98T>A NP_001252516.1:n.*98T>A
NM_005543.4:c.*81T>A MANE Select NP_005534.2:n.*81T>A
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