Canonical Allele Identifier: CA403668860

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117368A>T (hg19) ; chr19:g.7117357A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117357A>T , CM000681.2:g.7117357A>T	GRCh38
NC_000019.9:g.7117368A>T , CM000681.1:g.7117368A>T	GRCh37
NC_000019.8:g.7068368A>T	NCBI36
NG_008852.2:g.181644T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3848T>A MANE Select	ENSP00000303830.4:p.Phe1283Tyr
ENST00000302850.9:c.3848T>A	ENSP00000303830.4:p.Phe1283Tyr
ENST00000341500.9:c.3812T>A	ENSP00000342838.4:p.Phe1271Tyr
NM_000208.2:c.3848T>A	NP_000199.2:p.Phe1283Tyr
NM_000208.3:c.3848T>A	NP_000199.2:p.Phe1283Tyr
NM_001079817.1:c.3812T>A	NP_001073285.1:p.Phe1271Tyr
NM_001079817.2:c.3812T>A	NP_001073285.1:p.Phe1271Tyr
XM_011527988.1:c.3923T>A	XP_011526290.1:p.Phe1308Tyr
XM_011527989.1:c.3887T>A	XP_011526291.1:p.Phe1296Tyr
XM_011527988.2:c.3845T>A	XP_011526290.2:p.Phe1282Tyr
XM_011527989.3:c.3809T>A	XP_011526291.2:p.Phe1270Tyr
NM_000208.4:c.3848T>A MANE Select	NP_000199.2:p.Phe1283Tyr
NM_001079817.3:c.3812T>A	NP_001073285.1:p.Phe1271Tyr