Canonical Allele Identifier: CA403668704

Gene: INSR

Linked Data

• dbSNP Id: rs1301665267
• gnomAD v4: 19-7117288-C-T
• MyVariant Identifiers: chr19:g.7117299C>T (hg19) ; chr19:g.7117288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117288C>T , CM000681.2:g.7117288C>T	GRCh38
NC_000019.9:g.7117299C>T , CM000681.1:g.7117299C>T	GRCh37
NC_000019.8:g.7068299C>T	NCBI36
NG_008852.2:g.181713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3917G>A MANE Select	ENSP00000303830.4:p.Ser1306Asn
ENST00000302850.9:c.3917G>A	ENSP00000303830.4:p.Ser1306Asn
ENST00000341500.9:c.3881G>A	ENSP00000342838.4:p.Ser1294Asn
NM_000208.2:c.3917G>A	NP_000199.2:p.Ser1306Asn
NM_000208.3:c.3917G>A	NP_000199.2:p.Ser1306Asn
NM_001079817.1:c.3881G>A	NP_001073285.1:p.Ser1294Asn
NM_001079817.2:c.3881G>A	NP_001073285.1:p.Ser1294Asn
XM_011527988.1:c.3992G>A	XP_011526290.1:p.Ser1331Asn
XM_011527989.1:c.3956G>A	XP_011526291.1:p.Ser1319Asn
XM_011527988.2:c.3914G>A	XP_011526290.2:p.Ser1305Asn
XM_011527989.3:c.3878G>A	XP_011526291.2:p.Ser1293Asn
NM_000208.4:c.3917G>A MANE Select	NP_000199.2:p.Ser1306Asn
NM_001079817.3:c.3881G>A	NP_001073285.1:p.Ser1294Asn