Canonical Allele Identifier: CA505217398

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128919G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128908G>T , CM000681.2:g.7128908G>T	GRCh38
NC_000019.9:g.7128919G>T , CM000681.1:g.7128919G>T	GRCh37
NC_000019.8:g.7079919G>T	NCBI36
NG_008852.2:g.170093C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2889C>A MANE Select	ENSP00000303830.4:p.Ile963=
ENST00000302850.9:c.2889C>A	ENSP00000303830.4:p.Ile963=
ENST00000341500.9:c.2853C>A	ENSP00000342838.4:p.Ile951=
NM_000208.2:c.2889C>A	NP_000199.2:p.Ile963=
NM_000208.3:c.2889C>A	NP_000199.2:p.Ile963=
NM_001079817.1:c.2853C>A	NP_001073285.1:p.Ile951=
NM_001079817.2:c.2853C>A	NP_001073285.1:p.Ile951=
XM_011527988.1:c.2964C>A	XP_011526290.1:p.Ile988=
XM_011527989.1:c.2928C>A	XP_011526291.1:p.Ile976=
XM_011527988.2:c.2886C>A	XP_011526290.2:p.Ile962=
XM_011527989.3:c.2850C>A	XP_011526291.2:p.Ile950=
NM_000208.4:c.2889C>A MANE Select	NP_000199.2:p.Ile963=
NM_001079817.3:c.2853C>A	NP_001073285.1:p.Ile951=