Canonical Allele Identifier: CA505217682

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132308G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132297G>T , CM000681.2:g.7132297G>T	GRCh38
NC_000019.9:g.7132308G>T , CM000681.1:g.7132308G>T	GRCh37
NC_000019.8:g.7083308G>T	NCBI36
NG_008852.2:g.166704C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2703C>A MANE Select	ENSP00000303830.4:p.Ser901=
ENST00000302850.9:c.2703C>A	ENSP00000303830.4:p.Ser901=
ENST00000341500.9:c.2667C>A	ENSP00000342838.4:p.Ser889=
NM_000208.2:c.2703C>A	NP_000199.2:p.Ser901=
NM_000208.3:c.2703C>A	NP_000199.2:p.Ser901=
NM_001079817.1:c.2667C>A	NP_001073285.1:p.Ser889=
NM_001079817.2:c.2667C>A	NP_001073285.1:p.Ser889=
XM_011527988.1:c.2781C>A	XP_011526290.1:p.Ser927=
XM_011527989.1:c.2745C>A	XP_011526291.1:p.Ser915=
XM_011527988.2:c.2703C>A	XP_011526290.2:p.Ser901=
XM_011527989.3:c.2667C>A	XP_011526291.2:p.Ser889=
NM_000208.4:c.2703C>A MANE Select	NP_000199.2:p.Ser901=
NM_001079817.3:c.2667C>A	NP_001073285.1:p.Ser889=