Canonical Allele Identifier: CA2813449990

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7170816_7170817insA , CM000681.2:g.7170816_7170817insA	GRCh38
NC_000019.9:g.7170827_7170828insA , CM000681.1:g.7170827_7170828insA	GRCh37
NC_000019.8:g.7121827_7121828insA	NCBI36
NG_008852.2:g.128184_128185insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1269-66_1269-65insT MANE Select	ENSP00000303830.4:n.1269-66_1269-65insT
ENST00000302850.9:c.1269-66_1269-65insT	ENSP00000303830.4:n.1269-66_1269-65insT
ENST00000341500.9:c.1269-66_1269-65insT	ENSP00000342838.4:n.1269-66_1269-65insT
ENST00000598216.1:n.1244-66_1244-65insT
NM_000208.2:c.1269-66_1269-65insT	NP_000199.2:n.1269-66_1269-65insT
NM_000208.3:c.1269-66_1269-65insT	NP_000199.2:n.1269-66_1269-65insT
NM_001079817.1:c.1269-66_1269-65insT	NP_001073285.1:n.1269-66_1269-65insT
NM_001079817.2:c.1269-66_1269-65insT	NP_001073285.1:n.1269-66_1269-65insT
XM_011527988.1:c.1347-66_1347-65insT	XP_011526290.1:n.1347-66_1347-65insT
XM_011527989.1:c.1347-66_1347-65insT	XP_011526291.1:n.1347-66_1347-65insT
XM_011527988.2:c.1269-66_1269-65insT	XP_011526290.2:n.1269-66_1269-65insT
XM_011527989.3:c.1269-66_1269-65insT	XP_011526291.2:n.1269-66_1269-65insT
NM_000208.4:c.1269-66_1269-65insT MANE Select	NP_000199.2:n.1269-66_1269-65insT
NM_001079817.3:c.1269-66_1269-65insT	NP_001073285.1:n.1269-66_1269-65insT