Canonical Allele Identifier: CA993122689

Gene: INSR

Linked Data

• gnomAD v3: 19-7182908-C-CAAAAAA
• gnomAD v4: 19-7182908-C-CAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7182920_7182925dup , CM000681.2:g.7182920_7182925dup	GRCh38
NC_000019.9:g.7182931_7182936dup , CM000681.1:g.7182931_7182936dup	GRCh37
NC_000019.8:g.7133931_7133936dup	NCBI36
NG_008852.2:g.116087_116092dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.974+1402_974+1407dup MANE Select	ENSP00000303830.4:n.974+1402_974+1407dup
ENST00000302850.9:c.974+1402_974+1407dup	ENSP00000303830.4:n.974+1402_974+1407dup
ENST00000341500.9:c.974+1402_974+1407dup	ENSP00000342838.4:n.974+1402_974+1407dup
ENST00000598216.1:n.949+1402_949+1407dup
NM_000208.2:c.974+1402_974+1407dup	NP_000199.2:n.974+1402_974+1407dup
NM_000208.3:c.974+1402_974+1407dup	NP_000199.2:n.974+1402_974+1407dup
NM_001079817.1:c.974+1402_974+1407dup	NP_001073285.1:n.974+1402_974+1407dup
NM_001079817.2:c.974+1402_974+1407dup	NP_001073285.1:n.974+1402_974+1407dup
XM_011527988.1:c.1052+1402_1052+1407dup	XP_011526290.1:n.1052+1402_1052+1407dup
XM_011527989.1:c.1052+1402_1052+1407dup	XP_011526291.1:n.1052+1402_1052+1407dup
XM_011527988.2:c.974+1402_974+1407dup	XP_011526290.2:n.974+1402_974+1407dup
XM_011527989.3:c.974+1402_974+1407dup	XP_011526291.2:n.974+1402_974+1407dup
NM_000208.4:c.974+1402_974+1407dup MANE Select	NP_000199.2:n.974+1402_974+1407dup
NM_001079817.3:c.974+1402_974+1407dup	NP_001073285.1:n.974+1402_974+1407dup