Canonical Allele Identifier: CA1282466613

Gene: INSIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118102895C= , CM000664.2:g.118102895C=	GRCh38
NC_000002.11:g.118860471C= , CM000664.1:g.118860471C=	GRCh37
NC_000002.10:g.118576941C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245787.9:c.245-302C= MANE Select	ENSP00000245787.4:n.245-302C=
ENST00000245787.8:c.245-302C=	ENSP00000245787.4:n.245-302C=
ENST00000411929.5:c.-114-302C=	ENSP00000400126.1:n.-114-302C=
ENST00000467223.5:n.126-302C=
ENST00000471186.5:n.69-302C=
ENST00000485520.5:n.77-302C=
ENST00000488995.1:n.173+185C=
ENST00000614681.1:c.245-302C=	ENSP00000484179.1:n.245-302C=
NM_016133.2:c.245-302C=	NP_057217.2:n.245-302C=
XM_005263690.2:c.-80-302C=	XP_005263747.1:n.-80-302C=
XM_011511292.1:c.245-302C=	XP_011509594.1:n.245-302C=
NM_001321329.1:c.245-302C=	NP_001308258.1:n.245-302C=
NM_001321330.1:c.-80-302C=	NP_001308259.1:n.-80-302C=
NM_001321331.1:c.-80-302C=	NP_001308260.1:n.-80-302C=
NM_001321332.1:c.-80-302C=	NP_001308261.1:n.-80-302C=
NM_001321333.1:c.-80-302C=	NP_001308262.1:n.-80-302C=
NM_016133.3:c.245-302C=	NP_057217.2:n.245-302C=
NM_016133.4:c.245-302C= MANE Select	NP_057217.2:n.245-302C=
NM_001321329.2:c.245-302C=	NP_001308258.1:n.245-302C=
NM_001321330.2:c.-80-302C=	NP_001308259.1:n.-80-302C=
NM_001321331.2:c.-80-302C=	NP_001308260.1:n.-80-302C=
NM_001321332.2:c.-80-302C=	NP_001308261.1:n.-80-302C=
NM_001321333.2:c.-80-302C=	NP_001308262.1:n.-80-302C=