Canonical Allele Identifier: CA631680916

Gene: INSR

Linked Data

• gnomAD v2: 19-7212072-G-GTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAAT
• gnomAD v3: 19-7212061-G-GTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAAT
• gnomAD v4: 19-7212061-G-GTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAAT
• MyVariant Identifiers: chr19:g.7212072_7212073insTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAAT (hg19) ; chr19:g.7212061_7212062insTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212062_7212063insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATT , CM000681.2:g.7212062_7212063insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATT	GRCh38
NC_000019.9:g.7212073_7212074insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATT , CM000681.1:g.7212073_7212074insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATT	GRCh37
NC_000019.8:g.7163073_7163074insTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATT	NCBI36
NG_008852.2:g.86939_86940insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA MANE Select	ENSP00000303830.4:n.653-27425_653-27424insATTATCCACCCCAGAGTCT...
ENST00000302850.9:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	ENSP00000303830.4:n.653-27425_653-27424insATTATCCACCCCAGAGTCT...
ENST00000341500.9:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	ENSP00000342838.4:n.653-27425_653-27424insATTATCCACCCCAGAGTCT...
ENST00000598216.1:n.628-27425_628-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA
NM_000208.2:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	NP_000199.2:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCT...
NM_000208.3:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	NP_000199.2:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCT...
NM_001079817.1:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	NP_001073285.1:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAG...
NM_001079817.2:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	NP_001073285.1:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAG...
XM_011527988.1:c.731-27425_731-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	XP_011526290.1:n.731-27425_731-27424insATTATCCACCCCAGAGTCTGAG...
XM_011527989.1:c.731-27425_731-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	XP_011526291.1:n.731-27425_731-27424insATTATCCACCCCAGAGTCTGAG...
XM_011527988.2:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	XP_011526290.2:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAG...
XM_011527989.3:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	XP_011526291.2:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAG...
NM_000208.4:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA MANE Select	NP_000199.2:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCT...
NM_001079817.3:c.653-27425_653-27424insATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAA	NP_001073285.1:n.653-27425_653-27424insATTATCCACCCCAGAGTCTGAG...