Canonical Allele Identifier: CA505400253

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125456G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125445G>T , CM000681.2:g.7125445G>T	GRCh38
NC_000019.9:g.7125456G>T , CM000681.1:g.7125456G>T	GRCh37
NC_000019.8:g.7076456G>T	NCBI36
NG_008852.2:g.173556C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3096C>A MANE Select	ENSP00000303830.4:p.Gly1032=
ENST00000302850.9:c.3096C>A	ENSP00000303830.4:p.Gly1032=
ENST00000341500.9:c.3060C>A	ENSP00000342838.4:p.Gly1020=
NM_000208.2:c.3096C>A	NP_000199.2:p.Gly1032=
NM_000208.3:c.3096C>A	NP_000199.2:p.Gly1032=
NM_001079817.1:c.3060C>A	NP_001073285.1:p.Gly1020=
NM_001079817.2:c.3060C>A	NP_001073285.1:p.Gly1020=
XM_011527988.1:c.3171C>A	XP_011526290.1:p.Gly1057=
XM_011527989.1:c.3135C>A	XP_011526291.1:p.Gly1045=
XM_011527988.2:c.3093C>A	XP_011526290.2:p.Gly1031=
XM_011527989.3:c.3057C>A	XP_011526291.2:p.Gly1019=
NM_000208.4:c.3096C>A MANE Select	NP_000199.2:p.Gly1032=
NM_001079817.3:c.3060C>A	NP_001073285.1:p.Gly1020=