Canonical Allele Identifier: CA993105710
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125513_7125514insTTTTTT , CM000681.2:g.7125513_7125514insTTTTTT GRCh38
NC_000019.9:g.7125524_7125525insTTTTTT , CM000681.1:g.7125524_7125525insTTTTTT GRCh37
NC_000019.8:g.7076524_7076525insTTTTTT NCBI36
NG_008852.2:g.173487_173488insAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3027_3028insAAAAAA MANE Select ENSP00000303830.4:p.Ser1009_Val1010insLysLys
ENST00000302850.9:c.3027_3028insAAAAAA ENSP00000303830.4:p.Ser1009_Val1010insLysLys
ENST00000341500.9:c.2991_2992insAAAAAA ENSP00000342838.4:p.Ser997_Val998insLysLys
NM_000208.2:c.3027_3028insAAAAAA NP_000199.2:p.Ser1009_Val1010insLysLys
NM_000208.3:c.3027_3028insAAAAAA NP_000199.2:p.Ser1009_Val1010insLysLys
NM_001079817.1:c.2991_2992insAAAAAA NP_001073285.1:p.Ser997_Val998insLysLys
NM_001079817.2:c.2991_2992insAAAAAA NP_001073285.1:p.Ser997_Val998insLysLys
XM_011527988.1:c.3102_3103insAAAAAA XP_011526290.1:p.Ser1034_Val1035insLysLys
XM_011527989.1:c.3066_3067insAAAAAA XP_011526291.1:p.Ser1022_Val1023insLysLys
XM_011527988.2:c.3024_3025insAAAAAA XP_011526290.2:p.Ser1008_Val1009insLysLys
XM_011527989.3:c.2988_2989insAAAAAA XP_011526291.2:p.Ser996_Val997insLysLys
NM_000208.4:c.3027_3028insAAAAAA MANE Select NP_000199.2:p.Ser1009_Val1010insLysLys
NM_001079817.3:c.2991_2992insAAAAAA NP_001073285.1:p.Ser997_Val998insLysLys