Canonical Allele Identifier: CA993113320
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.2:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000019.9:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.1:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000019.8:g.7067732_7067733insAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_008852.2:g.182300_182301insTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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