Canonical Allele Identifier: CA403668466

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117197G>T (hg19) ; chr19:g.7117186G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117186G>T , CM000681.2:g.7117186G>T	GRCh38
NC_000019.9:g.7117197G>T , CM000681.1:g.7117197G>T	GRCh37
NC_000019.8:g.7068197G>T	NCBI36
NG_008852.2:g.181815C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4019C>A MANE Select	ENSP00000303830.4:p.Ala1340Glu
ENST00000302850.9:c.4019C>A	ENSP00000303830.4:p.Ala1340Glu
ENST00000341500.9:c.3983C>A	ENSP00000342838.4:p.Ala1328Glu
NM_000208.2:c.4019C>A	NP_000199.2:p.Ala1340Glu
NM_000208.3:c.4019C>A	NP_000199.2:p.Ala1340Glu
NM_001079817.1:c.3983C>A	NP_001073285.1:p.Ala1328Glu
NM_001079817.2:c.3983C>A	NP_001073285.1:p.Ala1328Glu
XM_011527988.1:c.4094C>A	XP_011526290.1:p.Ala1365Glu
XM_011527989.1:c.4058C>A	XP_011526291.1:p.Ala1353Glu
XM_011527988.2:c.4016C>A	XP_011526290.2:p.Ala1339Glu
XM_011527989.3:c.3980C>A	XP_011526291.2:p.Ala1327Glu
NM_000208.4:c.4019C>A MANE Select	NP_000199.2:p.Ala1340Glu
NM_001079817.3:c.3983C>A	NP_001073285.1:p.Ala1328Glu