Canonical Allele Identifier: CA783867978

Gene: INSL3

Linked Data

• dbSNP Id: rs1158390556
• gnomAD v3: 19-17818127-G-A
• gnomAD v4: 19-17818127-G-A
• MyVariant Identifiers: chr19:g.17928936G>A (hg19) ; chr19:g.17818127G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17818127G>A , CM000681.2:g.17818127G>A	GRCh38
NC_000019.9:g.17928936G>A , CM000681.1:g.17928936G>A	GRCh37
NC_000019.8:g.17789936G>A	NCBI36
NG_012092.1:g.8385C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317306.8:c.191-1068C>T MANE Select	ENSP00000321724.6:n.191-1068C>T
ENST00000317306.7:c.191-1068C>T	ENSP00000321724.6:n.191-1068C>T
ENST00000379695.5:c.286-1068C>T	ENSP00000369017.4:n.286-1068C>T
ENST00000598577.1:c.190-1046C>T
NM_001265587.1:c.286-1068C>T	NP_001252516.1:n.286-1068C>T
NM_005543.3:c.191-1068C>T	NP_005534.2:n.191-1068C>T
NM_001265587.2:c.286-1068C>T	NP_001252516.1:n.286-1068C>T
NM_005543.4:c.191-1068C>T MANE Select	NP_005534.2:n.191-1068C>T