Canonical Allele Identifier: CA783867975

Gene: INSL3

Linked Data

• dbSNP Id: rs1334987262
• gnomAD v3: 19-17818120-A-C
• gnomAD v4: 19-17818120-A-C
• MyVariant Identifiers: chr19:g.17928929A>C (hg19) ; chr19:g.17818120A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17818120A>C , CM000681.2:g.17818120A>C	GRCh38
NC_000019.9:g.17928929A>C , CM000681.1:g.17928929A>C	GRCh37
NC_000019.8:g.17789929A>C	NCBI36
NG_012092.1:g.8392T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317306.8:c.191-1061T>G MANE Select	ENSP00000321724.6:n.191-1061T>G
ENST00000317306.7:c.191-1061T>G	ENSP00000321724.6:n.191-1061T>G
ENST00000379695.5:c.286-1061T>G	ENSP00000369017.4:n.286-1061T>G
ENST00000598577.1:c.190-1039T>G
NM_001265587.1:c.286-1061T>G	NP_001252516.1:n.286-1061T>G
NM_005543.3:c.191-1061T>G	NP_005534.2:n.191-1061T>G
NM_001265587.2:c.286-1061T>G	NP_001252516.1:n.286-1061T>G
NM_005543.4:c.191-1061T>G MANE Select	NP_005534.2:n.191-1061T>G