Canonical Allele Identifier: CA2320796154
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1974379447

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184670_7184671insGAGAGG , CM000681.2:g.7184670_7184671insGAGAGG GRCh38
NC_000019.9:g.7184681_7184682insGAGAGG , CM000681.1:g.7184681_7184682insGAGAGG GRCh37
NC_000019.8:g.7135681_7135682insGAGAGG NCBI36
NG_008852.2:g.114330_114331insCCTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-34_653-33insCCTCTC MANE Select ENSP00000303830.4:n.653-34_653-33insCCTCTC
ENST00000302850.9:c.653-34_653-33insCCTCTC ENSP00000303830.4:n.653-34_653-33insCCTCTC
ENST00000341500.9:c.653-34_653-33insCCTCTC ENSP00000342838.4:n.653-34_653-33insCCTCTC
ENST00000598216.1:n.628-34_628-33insCCTCTC
NM_000208.2:c.653-34_653-33insCCTCTC NP_000199.2:n.653-34_653-33insCCTCTC
NM_000208.3:c.653-34_653-33insCCTCTC NP_000199.2:n.653-34_653-33insCCTCTC
NM_001079817.1:c.653-34_653-33insCCTCTC NP_001073285.1:n.653-34_653-33insCCTCTC
NM_001079817.2:c.653-34_653-33insCCTCTC NP_001073285.1:n.653-34_653-33insCCTCTC
XM_011527988.1:c.731-34_731-33insCCTCTC XP_011526290.1:n.731-34_731-33insCCTCTC
XM_011527989.1:c.731-34_731-33insCCTCTC XP_011526291.1:n.731-34_731-33insCCTCTC
XM_011527988.2:c.653-34_653-33insCCTCTC XP_011526290.2:n.653-34_653-33insCCTCTC
XM_011527989.3:c.653-34_653-33insCCTCTC XP_011526291.2:n.653-34_653-33insCCTCTC
NM_000208.4:c.653-34_653-33insCCTCTC MANE Select NP_000199.2:n.653-34_653-33insCCTCTC
NM_001079817.3:c.653-34_653-33insCCTCTC NP_001073285.1:n.653-34_653-33insCCTCTC