Canonical Allele Identifier: CA2320795442

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7182968_7182969delinsAC , CM000681.2:g.7182968_7182969delinsAC	GRCh38
NC_000019.9:g.7182979_7182980delinsAC , CM000681.1:g.7182979_7182980delinsAC	GRCh37
NC_000019.8:g.7133979_7133980delinsAC	NCBI36
NG_008852.2:g.116032_116033delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.974+1347_974+1348delinsGT MANE Select	ENSP00000303830.4:n.974+1347_974+1348delinsGT
ENST00000302850.9:c.974+1347_974+1348delinsGT	ENSP00000303830.4:n.974+1347_974+1348delinsGT
ENST00000341500.9:c.974+1347_974+1348delinsGT	ENSP00000342838.4:n.974+1347_974+1348delinsGT
ENST00000598216.1:n.949+1347_949+1348delinsGT
NM_000208.2:c.974+1347_974+1348delinsGT	NP_000199.2:n.974+1347_974+1348delinsGT
NM_000208.3:c.974+1347_974+1348delinsGT	NP_000199.2:n.974+1347_974+1348delinsGT
NM_001079817.1:c.974+1347_974+1348delinsGT	NP_001073285.1:n.974+1347_974+1348delinsGT
NM_001079817.2:c.974+1347_974+1348delinsGT	NP_001073285.1:n.974+1347_974+1348delinsGT
XM_011527988.1:c.1052+1347_1052+1348delinsGT	XP_011526290.1:n.1052+1347_1052+1348delinsGT
XM_011527989.1:c.1052+1347_1052+1348delinsGT	XP_011526291.1:n.1052+1347_1052+1348delinsGT
XM_011527988.2:c.974+1347_974+1348delinsGT	XP_011526290.2:n.974+1347_974+1348delinsGT
XM_011527989.3:c.974+1347_974+1348delinsGT	XP_011526291.2:n.974+1347_974+1348delinsGT
NM_000208.4:c.974+1347_974+1348delinsGT MANE Select	NP_000199.2:n.974+1347_974+1348delinsGT
NM_001079817.3:c.974+1347_974+1348delinsGT	NP_001073285.1:n.974+1347_974+1348delinsGT