Canonical Allele Identifier: CA505217135

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125300A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125289A>G , CM000681.2:g.7125289A>G	GRCh38
NC_000019.9:g.7125300A>G , CM000681.1:g.7125300A>G	GRCh37
NC_000019.8:g.7076300A>G	NCBI36
NG_008852.2:g.173712T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3252T>C MANE Select	ENSP00000303830.4:p.His1084=
ENST00000302850.9:c.3252T>C	ENSP00000303830.4:p.His1084=
ENST00000341500.9:c.3216T>C	ENSP00000342838.4:p.His1072=
ENST00000593970.1:n.98T>C
NM_000208.2:c.3252T>C	NP_000199.2:p.His1084=
NM_000208.3:c.3252T>C	NP_000199.2:p.His1084=
NM_001079817.1:c.3216T>C	NP_001073285.1:p.His1072=
NM_001079817.2:c.3216T>C	NP_001073285.1:p.His1072=
XM_011527988.1:c.3327T>C	XP_011526290.1:p.His1109=
XM_011527989.1:c.3291T>C	XP_011526291.1:p.His1097=
XM_011527988.2:c.3249T>C	XP_011526290.2:p.His1083=
XM_011527989.3:c.3213T>C	XP_011526291.2:p.His1071=
NM_000208.4:c.3252T>C MANE Select	NP_000199.2:p.His1084=
NM_001079817.3:c.3216T>C	NP_001073285.1:p.His1072=