Canonical Allele Identifier: CA9135440

Gene: INSR

Linked Data

• ClinVar Variation Id: 439838
• ClinVar RCV Id: RCV000507369
• dbSNP Id: rs35169098
• ExAC: 19:7132136 C / T
• gnomAD v2: 19-7132136-C-T
• gnomAD v3: 19-7132125-C-T
• gnomAD v4: 19-7132125-C-T
• MyVariant Identifiers: chr19:g.7132136C>T (hg19) ; chr19:g.7132125C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132125C>T , CM000681.2:g.7132125C>T	GRCh38
NC_000019.9:g.7132136C>T , CM000681.1:g.7132136C>T	GRCh37
NC_000019.8:g.7083136C>T	NCBI36
NG_008852.2:g.166876G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2842+33G>A MANE Select	ENSP00000303830.4:n.2842+33G>A
ENST00000302850.9:c.2842+33G>A	ENSP00000303830.4:n.2842+33G>A
ENST00000341500.9:c.2806+33G>A	ENSP00000342838.4:n.2806+33G>A
NM_000208.2:c.2842+33G>A	NP_000199.2:n.2842+33G>A
NM_000208.3:c.2842+33G>A	NP_000199.2:n.2842+33G>A
NM_001079817.1:c.2806+33G>A	NP_001073285.1:n.2806+33G>A
NM_001079817.2:c.2806+33G>A	NP_001073285.1:n.2806+33G>A
XM_011527988.1:c.2920+33G>A	XP_011526290.1:n.2920+33G>A
XM_011527989.1:c.2884+33G>A	XP_011526291.1:n.2884+33G>A
XM_011527988.2:c.2842+33G>A	XP_011526290.2:n.2842+33G>A
XM_011527989.3:c.2806+33G>A	XP_011526291.2:n.2806+33G>A
NM_000208.4:c.2842+33G>A MANE Select	NP_000199.2:n.2842+33G>A
NM_001079817.3:c.2806+33G>A	NP_001073285.1:n.2806+33G>A