Canonical Allele Identifier: CA505217665

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132293A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132282A>C , CM000681.2:g.7132282A>C	GRCh38
NC_000019.9:g.7132293A>C , CM000681.1:g.7132293A>C	GRCh37
NC_000019.8:g.7083293A>C	NCBI36
NG_008852.2:g.166719T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2718T>G MANE Select	ENSP00000303830.4:p.Ala906=
ENST00000302850.9:c.2718T>G	ENSP00000303830.4:p.Ala906=
ENST00000341500.9:c.2682T>G	ENSP00000342838.4:p.Ala894=
NM_000208.2:c.2718T>G	NP_000199.2:p.Ala906=
NM_000208.3:c.2718T>G	NP_000199.2:p.Ala906=
NM_001079817.1:c.2682T>G	NP_001073285.1:p.Ala894=
NM_001079817.2:c.2682T>G	NP_001073285.1:p.Ala894=
XM_011527988.1:c.2796T>G	XP_011526290.1:p.Ala932=
XM_011527989.1:c.2760T>G	XP_011526291.1:p.Ala920=
XM_011527988.2:c.2718T>G	XP_011526290.2:p.Ala906=
XM_011527989.3:c.2682T>G	XP_011526291.2:p.Ala894=
NM_000208.4:c.2718T>G MANE Select	NP_000199.2:p.Ala906=
NM_001079817.3:c.2682T>G	NP_001073285.1:p.Ala894=