Canonical Allele Identifier: CA403667652

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7172347A>C (hg19) ; chr19:g.7172336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172336A>C , CM000681.2:g.7172336A>C	GRCh38
NC_000019.9:g.7172347A>C , CM000681.1:g.7172347A>C	GRCh37
NC_000019.8:g.7123347A>C	NCBI36
NG_008852.2:g.126665T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1222T>G MANE Select	ENSP00000303830.4:p.Phe408Val
ENST00000302850.9:c.1222T>G	ENSP00000303830.4:p.Phe408Val
ENST00000341500.9:c.1222T>G	ENSP00000342838.4:p.Phe408Val
ENST00000598216.1:n.1197T>G
NM_000208.2:c.1222T>G	NP_000199.2:p.Phe408Val
NM_000208.3:c.1222T>G	NP_000199.2:p.Phe408Val
NM_001079817.1:c.1222T>G	NP_001073285.1:p.Phe408Val
NM_001079817.2:c.1222T>G	NP_001073285.1:p.Phe408Val
XM_011527988.1:c.1300T>G	XP_011526290.1:p.Phe434Val
XM_011527989.1:c.1300T>G	XP_011526291.1:p.Phe434Val
XM_011527988.2:c.1222T>G	XP_011526290.2:p.Phe408Val
XM_011527989.3:c.1222T>G	XP_011526291.2:p.Phe408Val
NM_000208.4:c.1222T>G MANE Select	NP_000199.2:p.Phe408Val
NM_001079817.3:c.1222T>G	NP_001073285.1:p.Phe408Val