Canonical Allele Identifier: CA505400367

Gene: INSR

Linked Data

• gnomAD v4: 19-7142979-C-T
• MyVariant Identifiers: chr19:g.7142990C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142979C>T , CM000681.2:g.7142979C>T	GRCh38
NC_000019.9:g.7142990C>T , CM000681.1:g.7142990C>T	GRCh37
NC_000019.8:g.7093990C>T	NCBI36
NG_008852.2:g.156022G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2379G>A MANE Select	ENSP00000303830.4:p.Glu793=
ENST00000302850.9:c.2379G>A	ENSP00000303830.4:p.Glu793=
ENST00000341500.9:c.2343G>A	ENSP00000342838.4:p.Glu781=
ENST00000597211.1:n.62G>A
NM_000208.2:c.2379G>A	NP_000199.2:p.Glu793=
NM_000208.3:c.2379G>A	NP_000199.2:p.Glu793=
NM_001079817.1:c.2343G>A	NP_001073285.1:p.Glu781=
NM_001079817.2:c.2343G>A	NP_001073285.1:p.Glu781=
XM_011527988.1:c.2457G>A	XP_011526290.1:p.Glu819=
XM_011527989.1:c.2421G>A	XP_011526291.1:p.Glu807=
XM_011527988.2:c.2379G>A	XP_011526290.2:p.Glu793=
XM_011527989.3:c.2343G>A	XP_011526291.2:p.Glu781=
NM_000208.4:c.2379G>A MANE Select	NP_000199.2:p.Glu793=
NM_001079817.3:c.2343G>A	NP_001073285.1:p.Glu781=