Canonical Allele Identifier: CA403671945

Gene: INSR

Linked Data

• gnomAD v4: 19-7132179-A-T
• MyVariant Identifiers: chr19:g.7132190A>T (hg19) ; chr19:g.7132179A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132179A>T , CM000681.2:g.7132179A>T	GRCh38
NC_000019.9:g.7132190A>T , CM000681.1:g.7132190A>T	GRCh37
NC_000019.8:g.7083190A>T	NCBI36
NG_008852.2:g.166822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2821T>A MANE Select	ENSP00000303830.4:p.Tyr941Asn
ENST00000302850.9:c.2821T>A	ENSP00000303830.4:p.Tyr941Asn
ENST00000341500.9:c.2785T>A	ENSP00000342838.4:p.Tyr929Asn
NM_000208.2:c.2821T>A	NP_000199.2:p.Tyr941Asn
NM_000208.3:c.2821T>A	NP_000199.2:p.Tyr941Asn
NM_001079817.1:c.2785T>A	NP_001073285.1:p.Tyr929Asn
NM_001079817.2:c.2785T>A	NP_001073285.1:p.Tyr929Asn
XM_011527988.1:c.2899T>A	XP_011526290.1:p.Tyr967Asn
XM_011527989.1:c.2863T>A	XP_011526291.1:p.Tyr955Asn
XM_011527988.2:c.2821T>A	XP_011526290.2:p.Tyr941Asn
XM_011527989.3:c.2785T>A	XP_011526291.2:p.Tyr929Asn
NM_000208.4:c.2821T>A MANE Select	NP_000199.2:p.Tyr941Asn
NM_001079817.3:c.2785T>A	NP_001073285.1:p.Tyr929Asn