Canonical Allele Identifier: CA2320769590

Gene: INSR

Linked Data

• dbSNP Id: rs1972718268

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7129156_7129159dup , CM000681.2:g.7129156_7129159dup	GRCh38
NC_000019.9:g.7129167_7129170dup , CM000681.1:g.7129167_7129170dup	GRCh37
NC_000019.8:g.7080167_7080170dup	NCBI36
NG_008852.2:g.169842_169845dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2843-205_2843-202dup MANE Select	ENSP00000303830.4:n.2843-205_2843-202dup
ENST00000302850.9:c.2843-205_2843-202dup	ENSP00000303830.4:n.2843-205_2843-202dup
ENST00000341500.9:c.2807-205_2807-202dup	ENSP00000342838.4:n.2807-205_2807-202dup
NM_000208.2:c.2843-205_2843-202dup	NP_000199.2:n.2843-205_2843-202dup
NM_000208.3:c.2843-205_2843-202dup	NP_000199.2:n.2843-205_2843-202dup
NM_001079817.1:c.2807-205_2807-202dup	NP_001073285.1:n.2807-205_2807-202dup
NM_001079817.2:c.2807-205_2807-202dup	NP_001073285.1:n.2807-205_2807-202dup
XM_011527988.1:c.2921-208_2921-205dup	XP_011526290.1:n.2921-208_2921-205dup
XM_011527989.1:c.2885-208_2885-205dup	XP_011526291.1:n.2885-208_2885-205dup
XM_011527988.2:c.2843-208_2843-205dup	XP_011526290.2:n.2843-208_2843-205dup
XM_011527989.3:c.2807-208_2807-205dup	XP_011526291.2:n.2807-208_2807-205dup
NM_000208.4:c.2843-205_2843-202dup MANE Select	NP_000199.2:n.2843-205_2843-202dup
NM_001079817.3:c.2807-205_2807-202dup	NP_001073285.1:n.2807-205_2807-202dup