Canonical Allele Identifier: CA993113316
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.2:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000019.9:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.1:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000019.8:g.7067732_7067733insAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_008852.2:g.182300_182301insTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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