Canonical Allele Identifier: CA2582314078

Gene: INSR

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.2:g.7116721_7116722insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000019.9:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000681.1:g.7116732_7116733insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000019.8:g.7067732_7067733insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_008852.2:g.182300_182301insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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