Canonical Allele Identifier: CA2841701814

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166424_7166425del , CM000681.2:g.7166424_7166425del	GRCh38
NC_000019.9:g.7166435_7166436del , CM000681.1:g.7166435_7166436del	GRCh37
NC_000019.8:g.7117435_7117436del	NCBI36
NG_008852.2:g.132577_132578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1611-20_1611-19del MANE Select	ENSP00000303830.4:n.1611-20_1611-19del
ENST00000302850.9:c.1611-20_1611-19del	ENSP00000303830.4:n.1611-20_1611-19del
ENST00000341500.9:c.1611-20_1611-19del	ENSP00000342838.4:n.1611-20_1611-19del
ENST00000598216.1:n.1586-20_1586-19del
ENST00000600492.1:c.12-20_12-19del	ENSP00000473170.1:n.12-20_12-19del
NM_000208.2:c.1611-20_1611-19del	NP_000199.2:n.1611-20_1611-19del
NM_000208.3:c.1611-20_1611-19del	NP_000199.2:n.1611-20_1611-19del
NM_001079817.1:c.1611-20_1611-19del	NP_001073285.1:n.1611-20_1611-19del
NM_001079817.2:c.1611-20_1611-19del	NP_001073285.1:n.1611-20_1611-19del
XM_011527988.1:c.1689-20_1689-19del	XP_011526290.1:n.1689-20_1689-19del
XM_011527989.1:c.1689-20_1689-19del	XP_011526291.1:n.1689-20_1689-19del
XM_011527988.2:c.1611-20_1611-19del	XP_011526290.2:n.1611-20_1611-19del
XM_011527989.3:c.1611-20_1611-19del	XP_011526291.2:n.1611-20_1611-19del
NM_000208.4:c.1611-20_1611-19del MANE Select	NP_000199.2:n.1611-20_1611-19del
NM_001079817.3:c.1611-20_1611-19del	NP_001073285.1:n.1611-20_1611-19del