Canonical Allele Identifier: CA403671000

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125310A>C (hg19) ; chr19:g.7125299A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125299A>C , CM000681.2:g.7125299A>C	GRCh38
NC_000019.9:g.7125310A>C , CM000681.1:g.7125310A>C	GRCh37
NC_000019.8:g.7076310A>C	NCBI36
NG_008852.2:g.173702T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3242T>G MANE Select	ENSP00000303830.4:p.Phe1081Cys
ENST00000302850.9:c.3242T>G	ENSP00000303830.4:p.Phe1081Cys
ENST00000341500.9:c.3206T>G	ENSP00000342838.4:p.Phe1069Cys
ENST00000593970.1:n.88T>G
NM_000208.2:c.3242T>G	NP_000199.2:p.Phe1081Cys
NM_000208.3:c.3242T>G	NP_000199.2:p.Phe1081Cys
NM_001079817.1:c.3206T>G	NP_001073285.1:p.Phe1069Cys
NM_001079817.2:c.3206T>G	NP_001073285.1:p.Phe1069Cys
XM_011527988.1:c.3317T>G	XP_011526290.1:p.Phe1106Cys
XM_011527989.1:c.3281T>G	XP_011526291.1:p.Phe1094Cys
XM_011527988.2:c.3239T>G	XP_011526290.2:p.Phe1080Cys
XM_011527989.3:c.3203T>G	XP_011526291.2:p.Phe1068Cys
NM_000208.4:c.3242T>G MANE Select	NP_000199.2:p.Phe1081Cys
NM_001079817.3:c.3206T>G	NP_001073285.1:p.Phe1069Cys