Canonical Allele Identifier: CA403670866

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122957A>T (hg19) ; chr19:g.7122946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122946A>T , CM000681.2:g.7122946A>T	GRCh38
NC_000019.9:g.7122957A>T , CM000681.1:g.7122957A>T	GRCh37
NC_000019.8:g.7073957A>T	NCBI36
NG_008852.2:g.176055T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3302T>A MANE Select	ENSP00000303830.4:p.Val1101Glu
ENST00000302850.9:c.3302T>A	ENSP00000303830.4:p.Val1101Glu
ENST00000341500.9:c.3266T>A	ENSP00000342838.4:p.Val1089Glu
ENST00000593970.1:n.148T>A
ENST00000601099.1:n.213T>A
NM_000208.2:c.3302T>A	NP_000199.2:p.Val1101Glu
NM_000208.3:c.3302T>A	NP_000199.2:p.Val1101Glu
NM_001079817.1:c.3266T>A	NP_001073285.1:p.Val1089Glu
NM_001079817.2:c.3266T>A	NP_001073285.1:p.Val1089Glu
XM_011527988.1:c.3377T>A	XP_011526290.1:p.Val1126Glu
XM_011527989.1:c.3341T>A	XP_011526291.1:p.Val1114Glu
XM_011527988.2:c.3299T>A	XP_011526290.2:p.Val1100Glu
XM_011527989.3:c.3263T>A	XP_011526291.2:p.Val1088Glu
NM_000208.4:c.3302T>A MANE Select	NP_000199.2:p.Val1101Glu
NM_001079817.3:c.3266T>A	NP_001073285.1:p.Val1089Glu