Canonical Allele Identifier: CA2320795434

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7182960_7182961delinsAT , CM000681.2:g.7182960_7182961delinsAT	GRCh38
NC_000019.9:g.7182971_7182972delinsAT , CM000681.1:g.7182971_7182972delinsAT	GRCh37
NC_000019.8:g.7133971_7133972delinsAT	NCBI36
NG_008852.2:g.116040_116041delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.974+1355_974+1356delinsAT MANE Select	ENSP00000303830.4:n.974+1355_974+1356delinsAT
ENST00000302850.9:c.974+1355_974+1356delinsAT	ENSP00000303830.4:n.974+1355_974+1356delinsAT
ENST00000341500.9:c.974+1355_974+1356delinsAT	ENSP00000342838.4:n.974+1355_974+1356delinsAT
ENST00000598216.1:n.949+1355_949+1356delinsAT
NM_000208.2:c.974+1355_974+1356delinsAT	NP_000199.2:n.974+1355_974+1356delinsAT
NM_000208.3:c.974+1355_974+1356delinsAT	NP_000199.2:n.974+1355_974+1356delinsAT
NM_001079817.1:c.974+1355_974+1356delinsAT	NP_001073285.1:n.974+1355_974+1356delinsAT
NM_001079817.2:c.974+1355_974+1356delinsAT	NP_001073285.1:n.974+1355_974+1356delinsAT
XM_011527988.1:c.1052+1355_1052+1356delinsAT	XP_011526290.1:n.1052+1355_1052+1356delinsAT
XM_011527989.1:c.1052+1355_1052+1356delinsAT	XP_011526291.1:n.1052+1355_1052+1356delinsAT
XM_011527988.2:c.974+1355_974+1356delinsAT	XP_011526290.2:n.974+1355_974+1356delinsAT
XM_011527989.3:c.974+1355_974+1356delinsAT	XP_011526291.2:n.974+1355_974+1356delinsAT
NM_000208.4:c.974+1355_974+1356delinsAT MANE Select	NP_000199.2:n.974+1355_974+1356delinsAT
NM_001079817.3:c.974+1355_974+1356delinsAT	NP_001073285.1:n.974+1355_974+1356delinsAT