Canonical Allele Identifier: CA403668812

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117345T>G (hg19) ; chr19:g.7117334T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117334T>G , CM000681.2:g.7117334T>G	GRCh38
NC_000019.9:g.7117345T>G , CM000681.1:g.7117345T>G	GRCh37
NC_000019.8:g.7068345T>G	NCBI36
NG_008852.2:g.181667A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3871A>C MANE Select	ENSP00000303830.4:p.Lys1291Gln
ENST00000302850.9:c.3871A>C	ENSP00000303830.4:p.Lys1291Gln
ENST00000341500.9:c.3835A>C	ENSP00000342838.4:p.Lys1279Gln
NM_000208.2:c.3871A>C	NP_000199.2:p.Lys1291Gln
NM_000208.3:c.3871A>C	NP_000199.2:p.Lys1291Gln
NM_001079817.1:c.3835A>C	NP_001073285.1:p.Lys1279Gln
NM_001079817.2:c.3835A>C	NP_001073285.1:p.Lys1279Gln
XM_011527988.1:c.3946A>C	XP_011526290.1:p.Lys1316Gln
XM_011527989.1:c.3910A>C	XP_011526291.1:p.Lys1304Gln
XM_011527988.2:c.3868A>C	XP_011526290.2:p.Lys1290Gln
XM_011527989.3:c.3832A>C	XP_011526291.2:p.Lys1278Gln
NM_000208.4:c.3871A>C MANE Select	NP_000199.2:p.Lys1291Gln
NM_001079817.3:c.3835A>C	NP_001073285.1:p.Lys1279Gln