Canonical Allele Identifier: CA505400235

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125417G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125406G>T , CM000681.2:g.7125406G>T	GRCh38
NC_000019.9:g.7125417G>T , CM000681.1:g.7125417G>T	GRCh37
NC_000019.8:g.7076417G>T	NCBI36
NG_008852.2:g.173595C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3135C>A MANE Select	ENSP00000303830.4:p.Ile1045=
ENST00000302850.9:c.3135C>A	ENSP00000303830.4:p.Ile1045=
ENST00000341500.9:c.3099C>A	ENSP00000342838.4:p.Ile1033=
NM_000208.2:c.3135C>A	NP_000199.2:p.Ile1045=
NM_000208.3:c.3135C>A	NP_000199.2:p.Ile1045=
NM_001079817.1:c.3099C>A	NP_001073285.1:p.Ile1033=
NM_001079817.2:c.3099C>A	NP_001073285.1:p.Ile1033=
XM_011527988.1:c.3210C>A	XP_011526290.1:p.Ile1070=
XM_011527989.1:c.3174C>A	XP_011526291.1:p.Ile1058=
XM_011527988.2:c.3132C>A	XP_011526290.2:p.Ile1044=
XM_011527989.3:c.3096C>A	XP_011526291.2:p.Ile1032=
NM_000208.4:c.3135C>A MANE Select	NP_000199.2:p.Ile1045=
NM_001079817.3:c.3099C>A	NP_001073285.1:p.Ile1033=