Canonical Allele Identifier: CA2513265810

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7170666_7170667insG , CM000681.2:g.7170666_7170667insG	GRCh38
NC_000019.9:g.7170677_7170678insG , CM000681.1:g.7170677_7170678insG	GRCh37
NC_000019.8:g.7121677_7121678insG	NCBI36
NG_008852.2:g.128334_128335insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1353_1354insC MANE Select	ENSP00000303830.4:p.Lys452GlnfsTer7
ENST00000302850.9:c.1353_1354insC	ENSP00000303830.4:p.Lys452GlnfsTer7
ENST00000341500.9:c.1353_1354insC	ENSP00000342838.4:p.Lys452GlnfsTer7
ENST00000598216.1:n.1328_1329insC
NM_000208.2:c.1353_1354insC	NP_000199.2:p.Lys452GlnfsTer7
NM_000208.3:c.1353_1354insC	NP_000199.2:p.Lys452GlnfsTer7
NM_001079817.1:c.1353_1354insC	NP_001073285.1:p.Lys452GlnfsTer7
NM_001079817.2:c.1353_1354insC	NP_001073285.1:p.Lys452GlnfsTer7
XM_011527988.1:c.1431_1432insC	XP_011526290.1:p.Lys478GlnfsTer7
XM_011527989.1:c.1431_1432insC	XP_011526291.1:p.Lys478GlnfsTer7
XM_011527988.2:c.1353_1354insC	XP_011526290.2:p.Lys452GlnfsTer7
XM_011527989.3:c.1353_1354insC	XP_011526291.2:p.Lys452GlnfsTer7
NM_000208.4:c.1353_1354insC MANE Select	NP_000199.2:p.Lys452GlnfsTer7
NM_001079817.3:c.1353_1354insC	NP_001073285.1:p.Lys452GlnfsTer7