Canonical Allele Identifier: CA993113317
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.2:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000019.9:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.1:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000019.8:g.7067732_7067733insAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_008852.2:g.182300_182301insTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000303830.4:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000302850.9:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000303830.4:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000341500.9:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000342838.4:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000208.2:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000199.2:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000208.3:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000199.2:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001079817.1:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001073285.1:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001079817.2:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001073285.1:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_011527988.1:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011526290.1:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_011527989.1:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011526291.1:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_011527988.2:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011526290.2:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_011527989.3:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011526291.2:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000208.4:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000199.2:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001079817.3:c.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001073285.1:n.*355_*356insTTTTTTTTTTTTTTTTTTTTTTTTTT