Canonical Allele Identifier: CA631680932
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7212064_7212065insCAGACTCTGGGG , CM000681.2:g.7212064_7212065insCAGACTCTGGGG GRCh38
NC_000019.9:g.7212075_7212076insCAGACTCTGGGG , CM000681.1:g.7212075_7212076insCAGACTCTGGGG GRCh37
NC_000019.8:g.7163075_7163076insCAGACTCTGGGG NCBI36
NG_008852.2:g.86936_86937insCCCCAGAGTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-27428_653-27427insCCCCAGAGTCTG MANE Select ENSP00000303830.4:n.653-27428_653-27427insCCCCAGAGTCTG
ENST00000302850.9:c.653-27428_653-27427insCCCCAGAGTCTG ENSP00000303830.4:n.653-27428_653-27427insCCCCAGAGTCTG
ENST00000341500.9:c.653-27428_653-27427insCCCCAGAGTCTG ENSP00000342838.4:n.653-27428_653-27427insCCCCAGAGTCTG
ENST00000598216.1:n.628-27428_628-27427insCCCCAGAGTCTG
NM_000208.2:c.653-27428_653-27427insCCCCAGAGTCTG NP_000199.2:n.653-27428_653-27427insCCCCAGAGTCTG
NM_000208.3:c.653-27428_653-27427insCCCCAGAGTCTG NP_000199.2:n.653-27428_653-27427insCCCCAGAGTCTG
NM_001079817.1:c.653-27428_653-27427insCCCCAGAGTCTG NP_001073285.1:n.653-27428_653-27427insCCCCAGAGTCTG
NM_001079817.2:c.653-27428_653-27427insCCCCAGAGTCTG NP_001073285.1:n.653-27428_653-27427insCCCCAGAGTCTG
XM_011527988.1:c.731-27428_731-27427insCCCCAGAGTCTG XP_011526290.1:n.731-27428_731-27427insCCCCAGAGTCTG
XM_011527989.1:c.731-27428_731-27427insCCCCAGAGTCTG XP_011526291.1:n.731-27428_731-27427insCCCCAGAGTCTG
XM_011527988.2:c.653-27428_653-27427insCCCCAGAGTCTG XP_011526290.2:n.653-27428_653-27427insCCCCAGAGTCTG
XM_011527989.3:c.653-27428_653-27427insCCCCAGAGTCTG XP_011526291.2:n.653-27428_653-27427insCCCCAGAGTCTG
NM_000208.4:c.653-27428_653-27427insCCCCAGAGTCTG MANE Select NP_000199.2:n.653-27428_653-27427insCCCCAGAGTCTG
NM_001079817.3:c.653-27428_653-27427insCCCCAGAGTCTG NP_001073285.1:n.653-27428_653-27427insCCCCAGAGTCTG