Canonical Allele Identifier: CA403666304

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7166224T>A (hg19) ; chr19:g.7166213T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166213T>A , CM000681.2:g.7166213T>A	GRCh38
NC_000019.9:g.7166224T>A , CM000681.1:g.7166224T>A	GRCh37
NC_000019.8:g.7117224T>A	NCBI36
NG_008852.2:g.132788A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1802A>T MANE Select	ENSP00000303830.4:p.Asp601Val
ENST00000302850.9:c.1802A>T	ENSP00000303830.4:p.Asp601Val
ENST00000341500.9:c.1802A>T	ENSP00000342838.4:p.Asp601Val
ENST00000598216.1:n.1777A>T
ENST00000600492.1:c.203A>T	ENSP00000473170.1:p.Asp68Val
NM_000208.2:c.1802A>T	NP_000199.2:p.Asp601Val
NM_000208.3:c.1802A>T	NP_000199.2:p.Asp601Val
NM_001079817.1:c.1802A>T	NP_001073285.1:p.Asp601Val
NM_001079817.2:c.1802A>T	NP_001073285.1:p.Asp601Val
XM_011527988.1:c.1880A>T	XP_011526290.1:p.Asp627Val
XM_011527989.1:c.1880A>T	XP_011526291.1:p.Asp627Val
XM_011527988.2:c.1802A>T	XP_011526290.2:p.Asp601Val
XM_011527989.3:c.1802A>T	XP_011526291.2:p.Asp601Val
NM_000208.4:c.1802A>T MANE Select	NP_000199.2:p.Asp601Val
NM_001079817.3:c.1802A>T	NP_001073285.1:p.Asp601Val