Canonical Allele Identifier: CA2813449732

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166539_7166540insCAACCAAACACACCCAACAC , CM000681.2:g.7166539_7166540insCAACCAAACACACCCAACAC	GRCh38
NC_000019.9:g.7166550_7166551insCAACCAAACACACCCAACAC , CM000681.1:g.7166550_7166551insCAACCAAACACACCCAACAC	GRCh37
NC_000019.8:g.7117550_7117551insCAACCAAACACACCCAACAC	NCBI36
NG_008852.2:g.132461_132462insGTGTTGGGTGTGTTTGGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG MANE Select	ENSP00000303830.4:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
ENST00000302850.9:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	ENSP00000303830.4:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
ENST00000341500.9:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	ENSP00000342838.4:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
ENST00000598216.1:n.1586-136_1586-135insGTGTTGGGTGTGTTTGGTTG
ENST00000600492.1:c.12-136_12-135insGTGTTGGGTGTGTTTGGTTG	ENSP00000473170.1:n.12-136_12-135insGTGTTGGGTGTGTTTGGTTG
NM_000208.2:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	NP_000199.2:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
NM_000208.3:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	NP_000199.2:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
NM_001079817.1:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	NP_001073285.1:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
NM_001079817.2:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	NP_001073285.1:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
XM_011527988.1:c.1689-136_1689-135insGTGTTGGGTGTGTTTGGTTG	XP_011526290.1:n.1689-136_1689-135insGTGTTGGGTGTGTTTGGTTG
XM_011527989.1:c.1689-136_1689-135insGTGTTGGGTGTGTTTGGTTG	XP_011526291.1:n.1689-136_1689-135insGTGTTGGGTGTGTTTGGTTG
XM_011527988.2:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	XP_011526290.2:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
XM_011527989.3:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	XP_011526291.2:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
NM_000208.4:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG MANE Select	NP_000199.2:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG
NM_001079817.3:c.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG	NP_001073285.1:n.1611-136_1611-135insGTGTTGGGTGTGTTTGGTTG