Canonical Allele Identifier: CA2832572907

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116725_7116726insAAG , CM000681.2:g.7116725_7116726insAAG	GRCh38
NC_000019.9:g.7116736_7116737insAAG , CM000681.1:g.7116736_7116737insAAG	GRCh37
NC_000019.8:g.7067736_7067737insAAG	NCBI36
NG_008852.2:g.182275_182276insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*330_*331insCTT MANE Select	ENSP00000303830.4:n.*330_*331insCTT
ENST00000302850.9:c.*330_*331insCTT	ENSP00000303830.4:n.*330_*331insCTT
ENST00000341500.9:c.*330_*331insCTT	ENSP00000342838.4:n.*330_*331insCTT
NM_000208.2:c.*330_*331insCTT	NP_000199.2:n.*330_*331insCTT
NM_000208.3:c.*330_*331insCTT	NP_000199.2:n.*330_*331insCTT
NM_001079817.1:c.*330_*331insCTT	NP_001073285.1:n.*330_*331insCTT
NM_001079817.2:c.*330_*331insCTT	NP_001073285.1:n.*330_*331insCTT
XM_011527988.1:c.*330_*331insCTT	XP_011526290.1:n.*330_*331insCTT
XM_011527989.1:c.*330_*331insCTT	XP_011526291.1:n.*330_*331insCTT
XM_011527988.2:c.*330_*331insCTT	XP_011526290.2:n.*330_*331insCTT
XM_011527989.3:c.*330_*331insCTT	XP_011526291.2:n.*330_*331insCTT
NM_000208.4:c.*330_*331insCTT MANE Select	NP_000199.2:n.*330_*331insCTT
NM_001079817.3:c.*330_*331insCTT	NP_001073285.1:n.*330_*331insCTT