Canonical Allele Identifier: CA505400229

Gene: INSR

Linked Data

• gnomAD v4: 19-7125394-C-T
• MyVariant Identifiers: chr19:g.7125405C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125394C>T , CM000681.2:g.7125394C>T	GRCh38
NC_000019.9:g.7125405C>T , CM000681.1:g.7125405C>T	GRCh37
NC_000019.8:g.7076405C>T	NCBI36
NG_008852.2:g.173607G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3147G>A MANE Select	ENSP00000303830.4:p.Glu1049=
ENST00000302850.9:c.3147G>A	ENSP00000303830.4:p.Glu1049=
ENST00000341500.9:c.3111G>A	ENSP00000342838.4:p.Glu1037=
NM_000208.2:c.3147G>A	NP_000199.2:p.Glu1049=
NM_000208.3:c.3147G>A	NP_000199.2:p.Glu1049=
NM_001079817.1:c.3111G>A	NP_001073285.1:p.Glu1037=
NM_001079817.2:c.3111G>A	NP_001073285.1:p.Glu1037=
XM_011527988.1:c.3222G>A	XP_011526290.1:p.Glu1074=
XM_011527989.1:c.3186G>A	XP_011526291.1:p.Glu1062=
XM_011527988.2:c.3144G>A	XP_011526290.2:p.Glu1048=
XM_011527989.3:c.3108G>A	XP_011526291.2:p.Glu1036=
NM_000208.4:c.3147G>A MANE Select	NP_000199.2:p.Glu1049=
NM_001079817.3:c.3111G>A	NP_001073285.1:p.Glu1037=