Canonical Allele Identifier: CA206380
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 211191
ClinVar RCV Id: RCV000193115
dbSNP Id: rs146698985

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7143065C>T , CM000681.2:g.7143065C>T GRCh38
NC_000019.9:g.7143076C>T , CM000681.1:g.7143076C>T GRCh37
NC_000019.8:g.7094076C>T NCBI36
NG_008852.2:g.155936G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2293G>A MANE Select ENSP00000303830.4:p.Gly765Ser
ENST00000302850.9:c.2293G>A ENSP00000303830.4:p.Gly765Ser
ENST00000341500.9:c.2257G>A ENSP00000342838.4:p.Gly753Ser
NM_000208.2:c.2293G>A NP_000199.2:p.Gly765Ser
NM_000208.3:c.2293G>A NP_000199.2:p.Gly765Ser
NM_001079817.1:c.2257G>A NP_001073285.1:p.Gly753Ser
NM_001079817.2:c.2257G>A NP_001073285.1:p.Gly753Ser
XM_011527988.1:c.2371G>A XP_011526290.1:p.Gly791Ser
XM_011527989.1:c.2335G>A XP_011526291.1:p.Gly779Ser
XM_011527988.2:c.2293G>A XP_011526290.2:p.Gly765Ser
XM_011527989.3:c.2257G>A XP_011526291.2:p.Gly753Ser
NM_000208.4:c.2293G>A MANE Select NP_000199.2:p.Gly765Ser
NM_001079817.3:c.2257G>A NP_001073285.1:p.Gly753Ser