Canonical Allele Identifier: CA403668208

Gene: INSR

Linked Data

• COSMIC: COSM4400129 ; COSM4400130
• MyVariant Identifiers: chr19:g.7117075G>A (hg19) ; chr19:g.7117064G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117064G>A , CM000681.2:g.7117064G>A	GRCh38
NC_000019.9:g.7117075G>A , CM000681.1:g.7117075G>A	GRCh37
NC_000019.8:g.7068075G>A	NCBI36
NG_008852.2:g.181937C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4141C>T MANE Select	ENSP00000303830.4:p.Pro1381Ser
ENST00000302850.9:c.4141C>T	ENSP00000303830.4:p.Pro1381Ser
ENST00000341500.9:c.4105C>T	ENSP00000342838.4:p.Pro1369Ser
NM_000208.2:c.4141C>T	NP_000199.2:p.Pro1381Ser
NM_000208.3:c.4141C>T	NP_000199.2:p.Pro1381Ser
NM_001079817.1:c.4105C>T	NP_001073285.1:p.Pro1369Ser
NM_001079817.2:c.4105C>T	NP_001073285.1:p.Pro1369Ser
XM_011527988.1:c.4216C>T	XP_011526290.1:p.Pro1406Ser
XM_011527989.1:c.4180C>T	XP_011526291.1:p.Pro1394Ser
XM_011527988.2:c.4138C>T	XP_011526290.2:p.Pro1380Ser
XM_011527989.3:c.4102C>T	XP_011526291.2:p.Pro1368Ser
NM_000208.4:c.4141C>T MANE Select	NP_000199.2:p.Pro1381Ser
NM_001079817.3:c.4105C>T	NP_001073285.1:p.Pro1369Ser