Canonical Allele Identifier: CA403669261

Gene: INSR

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119563C>T , CM000681.2:g.7119563C>T	GRCh38
NC_000019.9:g.7119574C>T , CM000681.1:g.7119574C>T	GRCh37
NC_000019.8:g.7070574C>T	NCBI36
NG_008852.2:g.179438G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3680G>A MANE Select	ENSP00000303830.4:p.Trp1227Ter
ENST00000302850.9:c.3680G>A	ENSP00000303830.4:p.Trp1227Ter
ENST00000341500.9:c.3644G>A	ENSP00000342838.4:p.Trp1215Ter
NM_000208.2:c.3680G>A	NP_000199.2:p.Trp1227Ter
NM_000208.3:c.3680G>A	NP_000199.2:p.Trp1227Ter
NM_001079817.1:c.3644G>A	NP_001073285.1:p.Trp1215Ter
NM_001079817.2:c.3644G>A	NP_001073285.1:p.Trp1215Ter
XM_011527988.1:c.3755G>A	XP_011526290.1:p.Trp1252Ter
XM_011527989.1:c.3719G>A	XP_011526291.1:p.Trp1240Ter
XM_011527988.2:c.3677G>A	XP_011526290.2:p.Trp1226Ter
XM_011527989.3:c.3641G>A	XP_011526291.2:p.Trp1214Ter
NM_000208.4:c.3680G>A MANE Select	NP_000199.2:p.Trp1227Ter
NM_001079817.3:c.3644G>A	NP_001073285.1:p.Trp1215Ter