Canonical Allele Identifier: CA403668198

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117069A>G (hg19) ; chr19:g.7117058A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117058A>G , CM000681.2:g.7117058A>G	GRCh38
NC_000019.9:g.7117069A>G , CM000681.1:g.7117069A>G	GRCh37
NC_000019.8:g.7068069A>G	NCBI36
NG_008852.2:g.181943T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4147T>C MANE Select	ENSP00000303830.4:p.Ter1383Gln
ENST00000302850.9:c.4147T>C	ENSP00000303830.4:p.Ter1383Gln
ENST00000341500.9:c.4111T>C	ENSP00000342838.4:p.Ter1371Gln
NM_000208.2:c.4147T>C	NP_000199.2:p.Ter1383Gln
NM_000208.3:c.4147T>C	NP_000199.2:p.Ter1383Gln
NM_001079817.1:c.4111T>C	NP_001073285.1:p.Ter1371Gln
NM_001079817.2:c.4111T>C	NP_001073285.1:p.Ter1371Gln
XM_011527988.1:c.4222T>C	XP_011526290.1:p.Ter1408Gln
XM_011527989.1:c.4186T>C	XP_011526291.1:p.Ter1396Gln
XM_011527988.2:c.4144T>C	XP_011526290.2:p.Ter1382Gln
XM_011527989.3:c.4108T>C	XP_011526291.2:p.Ter1370Gln
NM_000208.4:c.4147T>C MANE Select	NP_000199.2:p.Ter1383Gln
NM_001079817.3:c.4111T>C	NP_001073285.1:p.Ter1371Gln