Canonical Allele Identifier: CA2320790663

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172211_7172212delinsCA , CM000681.2:g.7172211_7172212delinsCA	GRCh38
NC_000019.9:g.7172222_7172223delinsCA , CM000681.1:g.7172222_7172223delinsCA	GRCh37
NC_000019.8:g.7123222_7123223delinsCA	NCBI36
NG_008852.2:g.126789_126790delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1268+78_1268+79delinsTG MANE Select	ENSP00000303830.4:n.1268+78_1268+79delinsTG
ENST00000302850.9:c.1268+78_1268+79delinsTG	ENSP00000303830.4:n.1268+78_1268+79delinsTG
ENST00000341500.9:c.1268+78_1268+79delinsTG	ENSP00000342838.4:n.1268+78_1268+79delinsTG
ENST00000598216.1:n.1243+78_1243+79delinsTG
NM_000208.2:c.1268+78_1268+79delinsTG	NP_000199.2:n.1268+78_1268+79delinsTG
NM_000208.3:c.1268+78_1268+79delinsTG	NP_000199.2:n.1268+78_1268+79delinsTG
NM_001079817.1:c.1268+78_1268+79delinsTG	NP_001073285.1:n.1268+78_1268+79delinsTG
NM_001079817.2:c.1268+78_1268+79delinsTG	NP_001073285.1:n.1268+78_1268+79delinsTG
XM_011527988.1:c.1346+78_1346+79delinsTG	XP_011526290.1:n.1346+78_1346+79delinsTG
XM_011527989.1:c.1346+78_1346+79delinsTG	XP_011526291.1:n.1346+78_1346+79delinsTG
XM_011527988.2:c.1268+78_1268+79delinsTG	XP_011526290.2:n.1268+78_1268+79delinsTG
XM_011527989.3:c.1268+78_1268+79delinsTG	XP_011526291.2:n.1268+78_1268+79delinsTG
NM_000208.4:c.1268+78_1268+79delinsTG MANE Select	NP_000199.2:n.1268+78_1268+79delinsTG
NM_001079817.3:c.1268+78_1268+79delinsTG	NP_001073285.1:n.1268+78_1268+79delinsTG