Canonical Allele Identifier: CA403668798

Gene: INSR

Linked Data

• gnomAD v4: 19-7117329-G-T
• MyVariant Identifiers: chr19:g.7117340G>T (hg19) ; chr19:g.7117329G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117329G>T , CM000681.2:g.7117329G>T	GRCh38
NC_000019.9:g.7117340G>T , CM000681.1:g.7117340G>T	GRCh37
NC_000019.8:g.7068340G>T	NCBI36
NG_008852.2:g.181672C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3876C>A MANE Select	ENSP00000303830.4:p.Asp1292Glu
ENST00000302850.9:c.3876C>A	ENSP00000303830.4:p.Asp1292Glu
ENST00000341500.9:c.3840C>A	ENSP00000342838.4:p.Asp1280Glu
NM_000208.2:c.3876C>A	NP_000199.2:p.Asp1292Glu
NM_000208.3:c.3876C>A	NP_000199.2:p.Asp1292Glu
NM_001079817.1:c.3840C>A	NP_001073285.1:p.Asp1280Glu
NM_001079817.2:c.3840C>A	NP_001073285.1:p.Asp1280Glu
XM_011527988.1:c.3951C>A	XP_011526290.1:p.Asp1317Glu
XM_011527989.1:c.3915C>A	XP_011526291.1:p.Asp1305Glu
XM_011527988.2:c.3873C>A	XP_011526290.2:p.Asp1291Glu
XM_011527989.3:c.3837C>A	XP_011526291.2:p.Asp1279Glu
NM_000208.4:c.3876C>A MANE Select	NP_000199.2:p.Asp1292Glu
NM_001079817.3:c.3840C>A	NP_001073285.1:p.Asp1280Glu