Canonical Allele Identifier: CA2320780941

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152607_7152608delinsAC , CM000681.2:g.7152607_7152608delinsAC	GRCh38
NC_000019.9:g.7152618_7152619delinsAC , CM000681.1:g.7152618_7152619delinsAC	GRCh37
NC_000019.8:g.7103618_7103619delinsAC	NCBI36
NG_008852.2:g.146393_146394delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+118_2231+119delinsGT MANE Select	ENSP00000303830.4:n.2231+118_2231+119delinsGT
ENST00000302850.9:c.2231+118_2231+119delinsGT	ENSP00000303830.4:n.2231+118_2231+119delinsGT
ENST00000341500.9:c.2231+118_2231+119delinsGT	ENSP00000342838.4:n.2231+118_2231+119delinsGT
ENST00000598216.1:n.2324_2325delinsGT
NM_000208.2:c.2231+118_2231+119delinsGT	NP_000199.2:n.2231+118_2231+119delinsGT
NM_000208.3:c.2231+118_2231+119delinsGT	NP_000199.2:n.2231+118_2231+119delinsGT
NM_001079817.1:c.2231+118_2231+119delinsGT	NP_001073285.1:n.2231+118_2231+119delinsGT
NM_001079817.2:c.2231+118_2231+119delinsGT	NP_001073285.1:n.2231+118_2231+119delinsGT
XM_011527988.1:c.2309+118_2309+119delinsGT	XP_011526290.1:n.2309+118_2309+119delinsGT
XM_011527989.1:c.2309+118_2309+119delinsGT	XP_011526291.1:n.2309+118_2309+119delinsGT
XM_011527988.2:c.2231+118_2231+119delinsGT	XP_011526290.2:n.2231+118_2231+119delinsGT
XM_011527989.3:c.2231+118_2231+119delinsGT	XP_011526291.2:n.2231+118_2231+119delinsGT
NM_000208.4:c.2231+118_2231+119delinsGT MANE Select	NP_000199.2:n.2231+118_2231+119delinsGT
NM_001079817.3:c.2231+118_2231+119delinsGT	NP_001073285.1:n.2231+118_2231+119delinsGT