Canonical Allele Identifier: CA884175382

Gene: INSR

Linked Data

• dbSNP Id: rs1282871883
• MyVariant Identifiers: chr19:g.7117292_7117294del (hg19) ; chr19:g.7117281_7117283del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117284_7117286del , CM000681.2:g.7117284_7117286del	GRCh38
NC_000019.9:g.7117295_7117297del , CM000681.1:g.7117295_7117297del	GRCh37
NC_000019.8:g.7068295_7068297del	NCBI36
NG_008852.2:g.181718_181720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3922_3924del MANE Select	ENSP00000303830.4:p.Glu1308del
ENST00000302850.9:c.3922_3924del	ENSP00000303830.4:p.Glu1308del
ENST00000341500.9:c.3886_3888del	ENSP00000342838.4:p.Glu1296del
NM_000208.2:c.3922_3924del	NP_000199.2:p.Glu1308del
NM_000208.3:c.3922_3924del	NP_000199.2:p.Glu1308del
NM_001079817.1:c.3886_3888del	NP_001073285.1:p.Glu1296del
NM_001079817.2:c.3886_3888del	NP_001073285.1:p.Glu1296del
XM_011527988.1:c.3997_3999del	XP_011526290.1:p.Glu1333del
XM_011527989.1:c.3961_3963del	XP_011526291.1:p.Glu1321del
XM_011527988.2:c.3919_3921del	XP_011526290.2:p.Glu1307del
XM_011527989.3:c.3883_3885del	XP_011526291.2:p.Glu1295del
NM_000208.4:c.3922_3924del MANE Select	NP_000199.2:p.Glu1308del
NM_001079817.3:c.3886_3888del	NP_001073285.1:p.Glu1296del