Canonical Allele Identifier: CA403670821

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122937G>T (hg19) ; chr19:g.7122926G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122926G>T , CM000681.2:g.7122926G>T	GRCh38
NC_000019.9:g.7122937G>T , CM000681.1:g.7122937G>T	GRCh37
NC_000019.8:g.7073937G>T	NCBI36
NG_008852.2:g.176075C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3322C>A MANE Select	ENSP00000303830.4:p.His1108Asn
ENST00000302850.9:c.3322C>A	ENSP00000303830.4:p.His1108Asn
ENST00000341500.9:c.3286C>A	ENSP00000342838.4:p.His1096Asn
ENST00000593970.1:n.168C>A
ENST00000601099.1:n.233C>A
NM_000208.2:c.3322C>A	NP_000199.2:p.His1108Asn
NM_000208.3:c.3322C>A	NP_000199.2:p.His1108Asn
NM_001079817.1:c.3286C>A	NP_001073285.1:p.His1096Asn
NM_001079817.2:c.3286C>A	NP_001073285.1:p.His1096Asn
XM_011527988.1:c.3397C>A	XP_011526290.1:p.His1133Asn
XM_011527989.1:c.3361C>A	XP_011526291.1:p.His1121Asn
XM_011527988.2:c.3319C>A	XP_011526290.2:p.His1107Asn
XM_011527989.3:c.3283C>A	XP_011526291.2:p.His1095Asn
NM_000208.4:c.3322C>A MANE Select	NP_000199.2:p.His1108Asn
NM_001079817.3:c.3286C>A	NP_001073285.1:p.His1096Asn