Canonical Allele Identifier: CA2320771005

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132068_7132070delinsTGC , CM000681.2:g.7132068_7132070delinsTGC	GRCh38
NC_000019.9:g.7132079_7132081delinsTGC , CM000681.1:g.7132079_7132081delinsTGC	GRCh37
NC_000019.8:g.7083079_7083081delinsTGC	NCBI36
NG_008852.2:g.166931_166933delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2842+88_2842+90delinsGCA MANE Select	ENSP00000303830.4:n.2842+88_2842+90delinsGCA
ENST00000302850.9:c.2842+88_2842+90delinsGCA	ENSP00000303830.4:n.2842+88_2842+90delinsGCA
ENST00000341500.9:c.2806+88_2806+90delinsGCA	ENSP00000342838.4:n.2806+88_2806+90delinsGCA
NM_000208.2:c.2842+88_2842+90delinsGCA	NP_000199.2:n.2842+88_2842+90delinsGCA
NM_000208.3:c.2842+88_2842+90delinsGCA	NP_000199.2:n.2842+88_2842+90delinsGCA
NM_001079817.1:c.2806+88_2806+90delinsGCA	NP_001073285.1:n.2806+88_2806+90delinsGCA
NM_001079817.2:c.2806+88_2806+90delinsGCA	NP_001073285.1:n.2806+88_2806+90delinsGCA
XM_011527988.1:c.2920+88_2920+90delinsGCA	XP_011526290.1:n.2920+88_2920+90delinsGCA
XM_011527989.1:c.2884+88_2884+90delinsGCA	XP_011526291.1:n.2884+88_2884+90delinsGCA
XM_011527988.2:c.2842+88_2842+90delinsGCA	XP_011526290.2:n.2842+88_2842+90delinsGCA
XM_011527989.3:c.2806+88_2806+90delinsGCA	XP_011526291.2:n.2806+88_2806+90delinsGCA
NM_000208.4:c.2842+88_2842+90delinsGCA MANE Select	NP_000199.2:n.2842+88_2842+90delinsGCA
NM_001079817.3:c.2806+88_2806+90delinsGCA	NP_001073285.1:n.2806+88_2806+90delinsGCA