Canonical Allele Identifier: CA403668269

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117107T>G (hg19) ; chr19:g.7117096T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117096T>G , CM000681.2:g.7117096T>G	GRCh38
NC_000019.9:g.7117107T>G , CM000681.1:g.7117107T>G	GRCh37
NC_000019.8:g.7068107T>G	NCBI36
NG_008852.2:g.181905A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4109A>C MANE Select	ENSP00000303830.4:p.Asn1370Thr
ENST00000302850.9:c.4109A>C	ENSP00000303830.4:p.Asn1370Thr
ENST00000341500.9:c.4073A>C	ENSP00000342838.4:p.Asn1358Thr
NM_000208.2:c.4109A>C	NP_000199.2:p.Asn1370Thr
NM_000208.3:c.4109A>C	NP_000199.2:p.Asn1370Thr
NM_001079817.1:c.4073A>C	NP_001073285.1:p.Asn1358Thr
NM_001079817.2:c.4073A>C	NP_001073285.1:p.Asn1358Thr
XM_011527988.1:c.4184A>C	XP_011526290.1:p.Asn1395Thr
XM_011527989.1:c.4148A>C	XP_011526291.1:p.Asn1383Thr
XM_011527988.2:c.4106A>C	XP_011526290.2:p.Asn1369Thr
XM_011527989.3:c.4070A>C	XP_011526291.2:p.Asn1357Thr
NM_000208.4:c.4109A>C MANE Select	NP_000199.2:p.Asn1370Thr
NM_001079817.3:c.4073A>C	NP_001073285.1:p.Asn1358Thr