Canonical Allele Identifier: CA403671813

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128933T>C (hg19) ; chr19:g.7128922T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128922T>C , CM000681.2:g.7128922T>C	GRCh38
NC_000019.9:g.7128933T>C , CM000681.1:g.7128933T>C	GRCh37
NC_000019.8:g.7079933T>C	NCBI36
NG_008852.2:g.170079A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2875A>G MANE Select	ENSP00000303830.4:p.Ile959Val
ENST00000302850.9:c.2875A>G	ENSP00000303830.4:p.Ile959Val
ENST00000341500.9:c.2839A>G	ENSP00000342838.4:p.Ile947Val
NM_000208.2:c.2875A>G	NP_000199.2:p.Ile959Val
NM_000208.3:c.2875A>G	NP_000199.2:p.Ile959Val
NM_001079817.1:c.2839A>G	NP_001073285.1:p.Ile947Val
NM_001079817.2:c.2839A>G	NP_001073285.1:p.Ile947Val
XM_011527988.1:c.2950A>G	XP_011526290.1:p.Ile984Val
XM_011527989.1:c.2914A>G	XP_011526291.1:p.Ile972Val
XM_011527988.2:c.2872A>G	XP_011526290.2:p.Ile958Val
XM_011527989.3:c.2836A>G	XP_011526291.2:p.Ile946Val
NM_000208.4:c.2875A>G MANE Select	NP_000199.2:p.Ile959Val
NM_001079817.3:c.2839A>G	NP_001073285.1:p.Ile947Val