Canonical Allele Identifier: CA993122755

Gene: INSR

Linked Data

• gnomAD v3: 19-7212062-T-TTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC
• gnomAD v4: 19-7212062-T-TTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212062_7212063insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC , CM000681.2:g.7212062_7212063insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC	GRCh38
NC_000019.9:g.7212073_7212074insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC , CM000681.1:g.7212073_7212074insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC	GRCh37
NC_000019.8:g.7163073_7163074insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTC	NCBI36
NG_008852.2:g.86938_86939insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA MANE Select	ENSP00000303830.4:n.653-27426_653-27425insGAATTATCCACCCCAGAGT...
ENST00000302850.9:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	ENSP00000303830.4:n.653-27426_653-27425insGAATTATCCACCCCAGAGT...
ENST00000341500.9:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	ENSP00000342838.4:n.653-27426_653-27425insGAATTATCCACCCCAGAGT...
ENST00000598216.1:n.628-27426_628-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA
NM_000208.2:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	NP_000199.2:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGT...
NM_000208.3:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	NP_000199.2:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGT...
NM_001079817.1:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	NP_001073285.1:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTG...
NM_001079817.2:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	NP_001073285.1:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTG...
XM_011527988.1:c.731-27426_731-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	XP_011526290.1:n.731-27426_731-27425insGAATTATCCACCCCAGAGTCTG...
XM_011527989.1:c.731-27426_731-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	XP_011526291.1:n.731-27426_731-27425insGAATTATCCACCCCAGAGTCTG...
XM_011527988.2:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	XP_011526290.2:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTG...
XM_011527989.3:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	XP_011526291.2:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTG...
NM_000208.4:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA MANE Select	NP_000199.2:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGT...
NM_001079817.3:c.653-27426_653-27425insGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAA	NP_001073285.1:n.653-27426_653-27425insGAATTATCCACCCCAGAGTCTG...