Canonical Allele Identifier: CA2320788150

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166032_7166034delinsTAA , CM000681.2:g.7166032_7166034delinsTAA	GRCh38
NC_000019.9:g.7166043_7166045delinsTAA , CM000681.1:g.7166043_7166045delinsTAA	GRCh37
NC_000019.8:g.7117043_7117045delinsTAA	NCBI36
NG_008852.2:g.132967_132969delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+120_1861+122delinsTTA MANE Select	ENSP00000303830.4:n.1861+120_1861+122delinsTTA
ENST00000302850.9:c.1861+120_1861+122delinsTTA	ENSP00000303830.4:n.1861+120_1861+122delinsTTA
ENST00000341500.9:c.1861+120_1861+122delinsTTA	ENSP00000342838.4:n.1861+120_1861+122delinsTTA
ENST00000598216.1:n.1836+120_1836+122delinsTTA
ENST00000600492.1:c.262+120_262+122delinsTTA	ENSP00000473170.1:n.262+120_262+122delinsTTA
NM_000208.2:c.1861+120_1861+122delinsTTA	NP_000199.2:n.1861+120_1861+122delinsTTA
NM_000208.3:c.1861+120_1861+122delinsTTA	NP_000199.2:n.1861+120_1861+122delinsTTA
NM_001079817.1:c.1861+120_1861+122delinsTTA	NP_001073285.1:n.1861+120_1861+122delinsTTA
NM_001079817.2:c.1861+120_1861+122delinsTTA	NP_001073285.1:n.1861+120_1861+122delinsTTA
XM_011527988.1:c.1939+120_1939+122delinsTTA	XP_011526290.1:n.1939+120_1939+122delinsTTA
XM_011527989.1:c.1939+120_1939+122delinsTTA	XP_011526291.1:n.1939+120_1939+122delinsTTA
XM_011527988.2:c.1861+120_1861+122delinsTTA	XP_011526290.2:n.1861+120_1861+122delinsTTA
XM_011527989.3:c.1861+120_1861+122delinsTTA	XP_011526291.2:n.1861+120_1861+122delinsTTA
NM_000208.4:c.1861+120_1861+122delinsTTA MANE Select	NP_000199.2:n.1861+120_1861+122delinsTTA
NM_001079817.3:c.1861+120_1861+122delinsTTA	NP_001073285.1:n.1861+120_1861+122delinsTTA