Canonical Allele Identifier: CA403668213

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117077T>G (hg19) ; chr19:g.7117066T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117066T>G , CM000681.2:g.7117066T>G	GRCh38
NC_000019.9:g.7117077T>G , CM000681.1:g.7117077T>G	GRCh37
NC_000019.8:g.7068077T>G	NCBI36
NG_008852.2:g.181935A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4139A>C MANE Select	ENSP00000303830.4:p.Asn1380Thr
ENST00000302850.9:c.4139A>C	ENSP00000303830.4:p.Asn1380Thr
ENST00000341500.9:c.4103A>C	ENSP00000342838.4:p.Asn1368Thr
NM_000208.2:c.4139A>C	NP_000199.2:p.Asn1380Thr
NM_000208.3:c.4139A>C	NP_000199.2:p.Asn1380Thr
NM_001079817.1:c.4103A>C	NP_001073285.1:p.Asn1368Thr
NM_001079817.2:c.4103A>C	NP_001073285.1:p.Asn1368Thr
XM_011527988.1:c.4214A>C	XP_011526290.1:p.Asn1405Thr
XM_011527989.1:c.4178A>C	XP_011526291.1:p.Asn1393Thr
XM_011527988.2:c.4136A>C	XP_011526290.2:p.Asn1379Thr
XM_011527989.3:c.4100A>C	XP_011526291.2:p.Asn1367Thr
NM_000208.4:c.4139A>C MANE Select	NP_000199.2:p.Asn1380Thr
NM_001079817.3:c.4103A>C	NP_001073285.1:p.Asn1368Thr