Canonical Allele Identifier: CA2956879264

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116960_7116961insTCCA , CM000681.2:g.7116960_7116961insTCCA	GRCh38
NC_000019.9:g.7116971_7116972insTCCA , CM000681.1:g.7116971_7116972insTCCA	GRCh37
NC_000019.8:g.7067971_7067972insTCCA	NCBI36
NG_008852.2:g.182040_182041insTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*95_*96insTGGA MANE Select	ENSP00000303830.4:n.*95_*96insTGGA
ENST00000302850.9:c.*95_*96insTGGA	ENSP00000303830.4:n.*95_*96insTGGA
ENST00000341500.9:c.*95_*96insTGGA	ENSP00000342838.4:n.*95_*96insTGGA
NM_000208.2:c.*95_*96insTGGA	NP_000199.2:n.*95_*96insTGGA
NM_000208.3:c.*95_*96insTGGA	NP_000199.2:n.*95_*96insTGGA
NM_001079817.1:c.*95_*96insTGGA	NP_001073285.1:n.*95_*96insTGGA
NM_001079817.2:c.*95_*96insTGGA	NP_001073285.1:n.*95_*96insTGGA
XM_011527988.1:c.*95_*96insTGGA	XP_011526290.1:n.*95_*96insTGGA
XM_011527989.1:c.*95_*96insTGGA	XP_011526291.1:n.*95_*96insTGGA
XM_011527988.2:c.*95_*96insTGGA	XP_011526290.2:n.*95_*96insTGGA
XM_011527989.3:c.*95_*96insTGGA	XP_011526291.2:n.*95_*96insTGGA
NM_000208.4:c.*95_*96insTGGA MANE Select	NP_000199.2:n.*95_*96insTGGA
NM_001079817.3:c.*95_*96insTGGA	NP_001073285.1:n.*95_*96insTGGA