Canonical Allele Identifier: CA14637818

Gene: INSL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17818178A>G , CM000681.2:g.17818178A>G	GRCh38
NC_000019.9:g.17928987A>G , CM000681.1:g.17928987A>G	GRCh37
NC_000019.8:g.17789987A>G	NCBI36
NG_012092.1:g.8334T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317306.8:c.191-1119T>C MANE Select	ENSP00000321724.6:n.191-1119T>C
ENST00000317306.7:c.191-1119T>C	ENSP00000321724.6:n.191-1119T>C
ENST00000379695.5:c.286-1119T>C	ENSP00000369017.4:n.286-1119T>C
ENST00000598577.1:c.190-1097T>C
NM_001265587.1:c.286-1119T>C	NP_001252516.1:n.286-1119T>C
NM_005543.3:c.191-1119T>C	NP_005534.2:n.191-1119T>C
NM_001265587.2:c.286-1119T>C	NP_001252516.1:n.286-1119T>C
NM_005543.4:c.191-1119T>C MANE Select	NP_005534.2:n.191-1119T>C