Canonical Allele Identifier: CA304844428

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7153196_7153197dup , CM000681.2:g.7153196_7153197dup	GRCh38
NC_000019.9:g.7153207_7153208dup , CM000681.1:g.7153207_7153208dup	GRCh37
NC_000019.8:g.7104207_7104208dup	NCBI36
NG_008852.2:g.145813_145814dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.2030-261_2030-260dup MANE Select	NP_000199.2:n.2030-261_2030-260dup
ENST00000302850.10:c.2030-261_2030-260dup MANE Select	ENSP00000303830.4:n.2030-261_2030-260dup
NM_000208.2:c.2030-261_2030-260dup	NP_000199.2:n.2030-261_2030-260dup
NM_000208.3:c.2030-261_2030-260dup	NP_000199.2:n.2030-261_2030-260dup
NM_001079817.1:c.2030-261_2030-260dup	NP_001073285.1:n.2030-261_2030-260dup
NM_001079817.2:c.2030-261_2030-260dup	NP_001073285.1:n.2030-261_2030-260dup
NM_001079817.3:c.2030-261_2030-260dup	NP_001073285.1:n.2030-261_2030-260dup
ENST00000302850.9:c.2030-261_2030-260dup	ENSP00000303830.4:n.2030-261_2030-260dup
ENST00000341500.9:c.2030-261_2030-260dup	ENSP00000342838.4:n.2030-261_2030-260dup
ENST00000598216.1:n.2005-261_2005-260dup
XM_011527988.1:c.2108-261_2108-260dup	XP_011526290.1:n.2108-261_2108-260dup
XM_011527988.2:c.2030-261_2030-260dup	XP_011526290.2:n.2030-261_2030-260dup
XM_011527989.1:c.2108-261_2108-260dup	XP_011526291.1:n.2108-261_2108-260dup
XM_011527989.3:c.2030-261_2030-260dup	XP_011526291.2:n.2030-261_2030-260dup