Canonical Allele Identifier: CA2320767919

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125332_7125333delinsTC , CM000681.2:g.7125332_7125333delinsTC	GRCh38
NC_000019.9:g.7125343_7125344delinsTC , CM000681.1:g.7125343_7125344delinsTC	GRCh37
NC_000019.8:g.7076343_7076344delinsTC	NCBI36
NG_008852.2:g.173668_173669delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3208_3209delinsGA MANE Select	ENSP00000303830.4:p.Glu1070=
ENST00000302850.9:c.3208_3209delinsGA	ENSP00000303830.4:p.Glu1070=
ENST00000341500.9:c.3172_3173delinsGA	ENSP00000342838.4:p.Glu1058=
ENST00000593970.1:n.54_55delinsGA
NM_000208.2:c.3208_3209delinsGA	NP_000199.2:p.Glu1070=
NM_000208.3:c.3208_3209delinsGA	NP_000199.2:p.Glu1070=
NM_001079817.1:c.3172_3173delinsGA	NP_001073285.1:p.Glu1058=
NM_001079817.2:c.3172_3173delinsGA	NP_001073285.1:p.Glu1058=
XM_011527988.1:c.3283_3284delinsGA	XP_011526290.1:p.Glu1095=
XM_011527989.1:c.3247_3248delinsGA	XP_011526291.1:p.Glu1083=
XM_011527988.2:c.3205_3206delinsGA	XP_011526290.2:p.Glu1069=
XM_011527989.3:c.3169_3170delinsGA	XP_011526291.2:p.Glu1057=
NM_000208.4:c.3208_3209delinsGA MANE Select	NP_000199.2:p.Glu1070=
NM_001079817.3:c.3172_3173delinsGA	NP_001073285.1:p.Glu1058=