Canonical Allele Identifier: CA755786645

Gene: INSIG2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118106298C>A , CM000664.2:g.118106298C>A	GRCh38
NC_000002.11:g.118863874C>A , CM000664.1:g.118863874C>A	GRCh37
NC_000002.10:g.118580344C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245787.9:c.370-439C>A MANE Select	ENSP00000245787.4:n.370-439C>A
ENST00000245787.8:c.370-439C>A	ENSP00000245787.4:n.370-439C>A
ENST00000411929.5:c.12-439C>A	ENSP00000400126.1:n.12-439C>A
ENST00000467223.5:n.251-439C>A
ENST00000471186.5:n.194-439C>A
ENST00000485520.5:n.202-439C>A
ENST00000488995.1:n.299-439C>A
ENST00000614681.1:c.370-439C>A	ENSP00000484179.1:n.370-439C>A
NM_016133.2:c.370-439C>A	NP_057217.2:n.370-439C>A
XM_005263690.2:c.46-439C>A	XP_005263747.1:n.46-439C>A
XM_011511292.1:c.370-439C>A	XP_011509594.1:n.370-439C>A
NM_001321329.1:c.370-439C>A	NP_001308258.1:n.370-439C>A
NM_001321330.1:c.46-439C>A	NP_001308259.1:n.46-439C>A
NM_001321331.1:c.46-439C>A	NP_001308260.1:n.46-439C>A
NM_001321332.1:c.46-439C>A	NP_001308261.1:n.46-439C>A
NM_001321333.1:c.46-439C>A	NP_001308262.1:n.46-439C>A
NM_016133.3:c.370-439C>A	NP_057217.2:n.370-439C>A
NM_016133.4:c.370-439C>A MANE Select	NP_057217.2:n.370-439C>A
NM_001321329.2:c.370-439C>A	NP_001308258.1:n.370-439C>A
NM_001321330.2:c.46-439C>A	NP_001308259.1:n.46-439C>A
NM_001321331.2:c.46-439C>A	NP_001308260.1:n.46-439C>A
NM_001321332.2:c.46-439C>A	NP_001308261.1:n.46-439C>A
NM_001321333.2:c.46-439C>A	NP_001308262.1:n.46-439C>A