Canonical Allele Identifier: CA403669366

Gene: INSR

Linked Data

• gnomAD v4: 19-7120644-A-T
• MyVariant Identifiers: chr19:g.7120655A>T (hg19) ; chr19:g.7120644A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120644A>T , CM000681.2:g.7120644A>T	GRCh38
NC_000019.9:g.7120655A>T , CM000681.1:g.7120655A>T	GRCh37
NC_000019.8:g.7071655A>T	NCBI36
NG_008852.2:g.178357T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3635T>A MANE Select	ENSP00000303830.4:p.Val1212Asp
ENST00000302850.9:c.3635T>A	ENSP00000303830.4:p.Val1212Asp
ENST00000341500.9:c.3599T>A	ENSP00000342838.4:p.Val1200Asp
ENST00000601099.1:n.546T>A
NM_000208.2:c.3635T>A	NP_000199.2:p.Val1212Asp
NM_000208.3:c.3635T>A	NP_000199.2:p.Val1212Asp
NM_001079817.1:c.3599T>A	NP_001073285.1:p.Val1200Asp
NM_001079817.2:c.3599T>A	NP_001073285.1:p.Val1200Asp
XM_011527988.1:c.3710T>A	XP_011526290.1:p.Val1237Asp
XM_011527989.1:c.3674T>A	XP_011526291.1:p.Val1225Asp
XM_011527988.2:c.3632T>A	XP_011526290.2:p.Val1211Asp
XM_011527989.3:c.3596T>A	XP_011526291.2:p.Val1199Asp
NM_000208.4:c.3635T>A MANE Select	NP_000199.2:p.Val1212Asp
NM_001079817.3:c.3599T>A	NP_001073285.1:p.Val1200Asp