Canonical Allele Identifier: CA2320788107

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7165927_7165928delinsGC , CM000681.2:g.7165927_7165928delinsGC	GRCh38
NC_000019.9:g.7165938_7165939delinsGC , CM000681.1:g.7165938_7165939delinsGC	GRCh37
NC_000019.8:g.7116938_7116939delinsGC	NCBI36
NG_008852.2:g.133073_133074delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+226_1861+227delinsGC MANE Select	ENSP00000303830.4:n.1861+226_1861+227delinsGC
ENST00000302850.9:c.1861+226_1861+227delinsGC	ENSP00000303830.4:n.1861+226_1861+227delinsGC
ENST00000341500.9:c.1861+226_1861+227delinsGC	ENSP00000342838.4:n.1861+226_1861+227delinsGC
ENST00000598216.1:n.1836+226_1836+227delinsGC
ENST00000600492.1:c.262+226_262+227delinsGC	ENSP00000473170.1:n.262+226_262+227delinsGC
NM_000208.2:c.1861+226_1861+227delinsGC	NP_000199.2:n.1861+226_1861+227delinsGC
NM_000208.3:c.1861+226_1861+227delinsGC	NP_000199.2:n.1861+226_1861+227delinsGC
NM_001079817.1:c.1861+226_1861+227delinsGC	NP_001073285.1:n.1861+226_1861+227delinsGC
NM_001079817.2:c.1861+226_1861+227delinsGC	NP_001073285.1:n.1861+226_1861+227delinsGC
XM_011527988.1:c.1939+226_1939+227delinsGC	XP_011526290.1:n.1939+226_1939+227delinsGC
XM_011527989.1:c.1939+226_1939+227delinsGC	XP_011526291.1:n.1939+226_1939+227delinsGC
XM_011527988.2:c.1861+226_1861+227delinsGC	XP_011526290.2:n.1861+226_1861+227delinsGC
XM_011527989.3:c.1861+226_1861+227delinsGC	XP_011526291.2:n.1861+226_1861+227delinsGC
NM_000208.4:c.1861+226_1861+227delinsGC MANE Select	NP_000199.2:n.1861+226_1861+227delinsGC
NM_001079817.3:c.1861+226_1861+227delinsGC	NP_001073285.1:n.1861+226_1861+227delinsGC