Canonical Allele Identifier: CA993113323

Gene: INSR

Linked Data

• gnomAD v3: 19-7116700-C-CAAAAAAAAAAAAAAAAAAAAAAAA
• gnomAD v4: 19-7116700-C-CAAAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.2:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000019.9:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.1:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000019.8:g.7067732_7067733insAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_008852.2:g.182300_182301insTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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