Canonical Allele Identifier: CA505400013

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117142G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117131G>A , CM000681.2:g.7117131G>A	GRCh38
NC_000019.9:g.7117142G>A , CM000681.1:g.7117142G>A	GRCh37
NC_000019.8:g.7068142G>A	NCBI36
NG_008852.2:g.181870C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4074C>T MANE Select	ENSP00000303830.4:p.His1358=
ENST00000302850.9:c.4074C>T	ENSP00000303830.4:p.His1358=
ENST00000341500.9:c.4038C>T	ENSP00000342838.4:p.His1346=
NM_000208.2:c.4074C>T	NP_000199.2:p.His1358=
NM_000208.3:c.4074C>T	NP_000199.2:p.His1358=
NM_001079817.1:c.4038C>T	NP_001073285.1:p.His1346=
NM_001079817.2:c.4038C>T	NP_001073285.1:p.His1346=
XM_011527988.1:c.4149C>T	XP_011526290.1:p.His1383=
XM_011527989.1:c.4113C>T	XP_011526291.1:p.His1371=
XM_011527988.2:c.4071C>T	XP_011526290.2:p.His1357=
XM_011527989.3:c.4035C>T	XP_011526291.2:p.His1345=
NM_000208.4:c.4074C>T MANE Select	NP_000199.2:p.His1358=
NM_001079817.3:c.4038C>T	NP_001073285.1:p.His1346=