Canonical Allele Identifier: CA2320790068

Gene: INSR

Linked Data

• dbSNP Id: rs1973999262

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7170772_7170775dup , CM000681.2:g.7170772_7170775dup	GRCh38
NC_000019.9:g.7170783_7170786dup , CM000681.1:g.7170783_7170786dup	GRCh37
NC_000019.8:g.7121783_7121786dup	NCBI36
NG_008852.2:g.128227_128230dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1269-23_1269-20dup MANE Select	ENSP00000303830.4:n.1269-23_1269-20dup
ENST00000302850.9:c.1269-23_1269-20dup	ENSP00000303830.4:n.1269-23_1269-20dup
ENST00000341500.9:c.1269-23_1269-20dup	ENSP00000342838.4:n.1269-23_1269-20dup
ENST00000598216.1:n.1244-23_1244-20dup
NM_000208.2:c.1269-23_1269-20dup	NP_000199.2:n.1269-23_1269-20dup
NM_000208.3:c.1269-23_1269-20dup	NP_000199.2:n.1269-23_1269-20dup
NM_001079817.1:c.1269-23_1269-20dup	NP_001073285.1:n.1269-23_1269-20dup
NM_001079817.2:c.1269-23_1269-20dup	NP_001073285.1:n.1269-23_1269-20dup
XM_011527988.1:c.1347-23_1347-20dup	XP_011526290.1:n.1347-23_1347-20dup
XM_011527989.1:c.1347-23_1347-20dup	XP_011526291.1:n.1347-23_1347-20dup
XM_011527988.2:c.1269-23_1269-20dup	XP_011526290.2:n.1269-23_1269-20dup
XM_011527989.3:c.1269-23_1269-20dup	XP_011526291.2:n.1269-23_1269-20dup
NM_000208.4:c.1269-23_1269-20dup MANE Select	NP_000199.2:n.1269-23_1269-20dup
NM_001079817.3:c.1269-23_1269-20dup	NP_001073285.1:n.1269-23_1269-20dup