Canonical Allele Identifier: CA2320796066

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184275_7184278delinsTCTC , CM000681.2:g.7184275_7184278delinsTCTC	GRCh38
NC_000019.9:g.7184286_7184289delinsTCTC , CM000681.1:g.7184286_7184289delinsTCTC	GRCh37
NC_000019.8:g.7135286_7135289delinsTCTC	NCBI36
NG_008852.2:g.114723_114726delinsGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.974+38_974+41delinsGAGA MANE Select	ENSP00000303830.4:n.974+38_974+41delinsGAGA
ENST00000302850.9:c.974+38_974+41delinsGAGA	ENSP00000303830.4:n.974+38_974+41delinsGAGA
ENST00000341500.9:c.974+38_974+41delinsGAGA	ENSP00000342838.4:n.974+38_974+41delinsGAGA
ENST00000598216.1:n.949+38_949+41delinsGAGA
NM_000208.2:c.974+38_974+41delinsGAGA	NP_000199.2:n.974+38_974+41delinsGAGA
NM_000208.3:c.974+38_974+41delinsGAGA	NP_000199.2:n.974+38_974+41delinsGAGA
NM_001079817.1:c.974+38_974+41delinsGAGA	NP_001073285.1:n.974+38_974+41delinsGAGA
NM_001079817.2:c.974+38_974+41delinsGAGA	NP_001073285.1:n.974+38_974+41delinsGAGA
XM_011527988.1:c.1052+38_1052+41delinsGAGA	XP_011526290.1:n.1052+38_1052+41delinsGAGA
XM_011527989.1:c.1052+38_1052+41delinsGAGA	XP_011526291.1:n.1052+38_1052+41delinsGAGA
XM_011527988.2:c.974+38_974+41delinsGAGA	XP_011526290.2:n.974+38_974+41delinsGAGA
XM_011527989.3:c.974+38_974+41delinsGAGA	XP_011526291.2:n.974+38_974+41delinsGAGA
NM_000208.4:c.974+38_974+41delinsGAGA MANE Select	NP_000199.2:n.974+38_974+41delinsGAGA
NM_001079817.3:c.974+38_974+41delinsGAGA	NP_001073285.1:n.974+38_974+41delinsGAGA