Canonical Allele Identifier: CA505217366

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128874G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128863G>A , CM000681.2:g.7128863G>A	GRCh38
NC_000019.9:g.7128874G>A , CM000681.1:g.7128874G>A	GRCh37
NC_000019.8:g.7079874G>A	NCBI36
NG_008852.2:g.170138C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2934C>T MANE Select	ENSP00000303830.4:p.Phe978=
ENST00000302850.9:c.2934C>T	ENSP00000303830.4:p.Phe978=
ENST00000341500.9:c.2898C>T	ENSP00000342838.4:p.Phe966=
NM_000208.2:c.2934C>T	NP_000199.2:p.Phe978=
NM_000208.3:c.2934C>T	NP_000199.2:p.Phe978=
NM_001079817.1:c.2898C>T	NP_001073285.1:p.Phe966=
NM_001079817.2:c.2898C>T	NP_001073285.1:p.Phe966=
XM_011527988.1:c.3009C>T	XP_011526290.1:p.Phe1003=
XM_011527989.1:c.2973C>T	XP_011526291.1:p.Phe991=
XM_011527988.2:c.2931C>T	XP_011526290.2:p.Phe977=
XM_011527989.3:c.2895C>T	XP_011526291.2:p.Phe965=
NM_000208.4:c.2934C>T MANE Select	NP_000199.2:p.Phe978=
NM_001079817.3:c.2898C>T	NP_001073285.1:p.Phe966=