Canonical Allele Identifier: CA2320780926

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152584_7152585delinsAC , CM000681.2:g.7152584_7152585delinsAC	GRCh38
NC_000019.9:g.7152595_7152596delinsAC , CM000681.1:g.7152595_7152596delinsAC	GRCh37
NC_000019.8:g.7103595_7103596delinsAC	NCBI36
NG_008852.2:g.146416_146417delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+141_2231+142delinsGT MANE Select	ENSP00000303830.4:n.2231+141_2231+142delinsGT
ENST00000302850.9:c.2231+141_2231+142delinsGT	ENSP00000303830.4:n.2231+141_2231+142delinsGT
ENST00000341500.9:c.2231+141_2231+142delinsGT	ENSP00000342838.4:n.2231+141_2231+142delinsGT
ENST00000598216.1:n.2347_2348delinsGT
NM_000208.2:c.2231+141_2231+142delinsGT	NP_000199.2:n.2231+141_2231+142delinsGT
NM_000208.3:c.2231+141_2231+142delinsGT	NP_000199.2:n.2231+141_2231+142delinsGT
NM_001079817.1:c.2231+141_2231+142delinsGT	NP_001073285.1:n.2231+141_2231+142delinsGT
NM_001079817.2:c.2231+141_2231+142delinsGT	NP_001073285.1:n.2231+141_2231+142delinsGT
XM_011527988.1:c.2309+141_2309+142delinsGT	XP_011526290.1:n.2309+141_2309+142delinsGT
XM_011527989.1:c.2309+141_2309+142delinsGT	XP_011526291.1:n.2309+141_2309+142delinsGT
XM_011527988.2:c.2231+141_2231+142delinsGT	XP_011526290.2:n.2231+141_2231+142delinsGT
XM_011527989.3:c.2231+141_2231+142delinsGT	XP_011526291.2:n.2231+141_2231+142delinsGT
NM_000208.4:c.2231+141_2231+142delinsGT MANE Select	NP_000199.2:n.2231+141_2231+142delinsGT
NM_001079817.3:c.2231+141_2231+142delinsGT	NP_001073285.1:n.2231+141_2231+142delinsGT