Canonical Allele Identifier: CA2695228091

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132247_7132248delinsCA , CM000681.2:g.7132247_7132248delinsCA	GRCh38
NC_000019.9:g.7132258_7132259delinsCA , CM000681.1:g.7132258_7132259delinsCA	GRCh37
NC_000019.8:g.7083258_7083259delinsCA	NCBI36
NG_008852.2:g.166753_166754delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2752_2753delinsTG MANE Select	ENSP00000303830.4:p.Pro918Trp
ENST00000302850.9:c.2752_2753delinsTG	ENSP00000303830.4:p.Pro918Trp
ENST00000341500.9:c.2716_2717delinsTG	ENSP00000342838.4:p.Pro906Trp
NM_000208.2:c.2752_2753delinsTG	NP_000199.2:p.Pro918Trp
NM_000208.3:c.2752_2753delinsTG	NP_000199.2:p.Pro918Trp
NM_001079817.1:c.2716_2717delinsTG	NP_001073285.1:p.Pro906Trp
NM_001079817.2:c.2716_2717delinsTG	NP_001073285.1:p.Pro906Trp
XM_011527988.1:c.2830_2831delinsTG	XP_011526290.1:p.Pro944Trp
XM_011527989.1:c.2794_2795delinsTG	XP_011526291.1:p.Pro932Trp
XM_011527988.2:c.2752_2753delinsTG	XP_011526290.2:p.Pro918Trp
XM_011527989.3:c.2716_2717delinsTG	XP_011526291.2:p.Pro906Trp
NM_000208.4:c.2752_2753delinsTG MANE Select	NP_000199.2:p.Pro918Trp
NM_001079817.3:c.2716_2717delinsTG	NP_001073285.1:p.Pro906Trp