Canonical Allele Identifier: CA2832572909

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117184_7117185dup , CM000681.2:g.7117184_7117185dup	GRCh38
NC_000019.9:g.7117195_7117196dup , CM000681.1:g.7117195_7117196dup	GRCh37
NC_000019.8:g.7068195_7068196dup	NCBI36
NG_008852.2:g.181820_181821dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4024_4025dup MANE Select	ENSP00000303830.4:p.Arg1343AlafsTer23
ENST00000302850.9:c.4024_4025dup	ENSP00000303830.4:p.Arg1343AlafsTer23
ENST00000341500.9:c.3988_3989dup	ENSP00000342838.4:p.Arg1331AlafsTer23
NM_000208.2:c.4024_4025dup	NP_000199.2:p.Arg1343AlafsTer23
NM_000208.3:c.4024_4025dup	NP_000199.2:p.Arg1343AlafsTer23
NM_001079817.1:c.3988_3989dup	NP_001073285.1:p.Arg1331AlafsTer23
NM_001079817.2:c.3988_3989dup	NP_001073285.1:p.Arg1331AlafsTer23
XM_011527988.1:c.4099_4100dup	XP_011526290.1:p.Arg1368AlafsTer23
XM_011527989.1:c.4063_4064dup	XP_011526291.1:p.Arg1356AlafsTer23
XM_011527988.2:c.4021_4022dup	XP_011526290.2:p.Arg1342AlafsTer23
XM_011527989.3:c.3985_3986dup	XP_011526291.2:p.Arg1330AlafsTer23
NM_000208.4:c.4024_4025dup MANE Select	NP_000199.2:p.Arg1343AlafsTer23
NM_001079817.3:c.3988_3989dup	NP_001073285.1:p.Arg1331AlafsTer23