Canonical Allele Identifier: CA2587920829

Gene: INSR

Linked Data

• gnomAD v4: 19-7116859-C-CCTGTGAACCTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116859_7116860insCTGTGAACCTGG , CM000681.2:g.7116859_7116860insCTGTGAACCTGG	GRCh38
NC_000019.9:g.7116870_7116871insCTGTGAACCTGG , CM000681.1:g.7116870_7116871insCTGTGAACCTGG	GRCh37
NC_000019.8:g.7067870_7067871insCTGTGAACCTGG	NCBI36
NG_008852.2:g.182141_182142insCCAGGTTCACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*196_*197insCCAGGTTCACAG MANE Select	ENSP00000303830.4:n.*196_*197insCCAGGTTCACAG
ENST00000302850.9:c.*196_*197insCCAGGTTCACAG	ENSP00000303830.4:n.*196_*197insCCAGGTTCACAG
ENST00000341500.9:c.*196_*197insCCAGGTTCACAG	ENSP00000342838.4:n.*196_*197insCCAGGTTCACAG
NM_000208.2:c.*196_*197insCCAGGTTCACAG	NP_000199.2:n.*196_*197insCCAGGTTCACAG
NM_000208.3:c.*196_*197insCCAGGTTCACAG	NP_000199.2:n.*196_*197insCCAGGTTCACAG
NM_001079817.1:c.*196_*197insCCAGGTTCACAG	NP_001073285.1:n.*196_*197insCCAGGTTCACAG
NM_001079817.2:c.*196_*197insCCAGGTTCACAG	NP_001073285.1:n.*196_*197insCCAGGTTCACAG
XM_011527988.1:c.*196_*197insCCAGGTTCACAG	XP_011526290.1:n.*196_*197insCCAGGTTCACAG
XM_011527989.1:c.*196_*197insCCAGGTTCACAG	XP_011526291.1:n.*196_*197insCCAGGTTCACAG
XM_011527988.2:c.*196_*197insCCAGGTTCACAG	XP_011526290.2:n.*196_*197insCCAGGTTCACAG
XM_011527989.3:c.*196_*197insCCAGGTTCACAG	XP_011526291.2:n.*196_*197insCCAGGTTCACAG
NM_000208.4:c.*196_*197insCCAGGTTCACAG MANE Select	NP_000199.2:n.*196_*197insCCAGGTTCACAG
NM_001079817.3:c.*196_*197insCCAGGTTCACAG	NP_001073285.1:n.*196_*197insCCAGGTTCACAG