Canonical Allele Identifier: CA403668274

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117108T>C (hg19) ; chr19:g.7117097T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117097T>C , CM000681.2:g.7117097T>C	GRCh38
NC_000019.9:g.7117108T>C , CM000681.1:g.7117108T>C	GRCh37
NC_000019.8:g.7068108T>C	NCBI36
NG_008852.2:g.181904A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4108A>G MANE Select	ENSP00000303830.4:p.Asn1370Asp
ENST00000302850.9:c.4108A>G	ENSP00000303830.4:p.Asn1370Asp
ENST00000341500.9:c.4072A>G	ENSP00000342838.4:p.Asn1358Asp
NM_000208.2:c.4108A>G	NP_000199.2:p.Asn1370Asp
NM_000208.3:c.4108A>G	NP_000199.2:p.Asn1370Asp
NM_001079817.1:c.4072A>G	NP_001073285.1:p.Asn1358Asp
NM_001079817.2:c.4072A>G	NP_001073285.1:p.Asn1358Asp
XM_011527988.1:c.4183A>G	XP_011526290.1:p.Asn1395Asp
XM_011527989.1:c.4147A>G	XP_011526291.1:p.Asn1383Asp
XM_011527988.2:c.4105A>G	XP_011526290.2:p.Asn1369Asp
XM_011527989.3:c.4069A>G	XP_011526291.2:p.Asn1357Asp
NM_000208.4:c.4108A>G MANE Select	NP_000199.2:p.Asn1370Asp
NM_001079817.3:c.4072A>G	NP_001073285.1:p.Asn1358Asp