Canonical Allele Identifier: CA9135359

Gene: INSR

Linked Data

• dbSNP Id: rs764479879
• ExAC: 19:7125449 C / T
• gnomAD v2: 19-7125449-C-T
• gnomAD v3: 19-7125438-C-T
• gnomAD v4: 19-7125438-C-T
• MyVariant Identifiers: chr19:g.7125449C>T (hg19) ; chr19:g.7125438C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125438C>T , CM000681.2:g.7125438C>T	GRCh38
NC_000019.9:g.7125449C>T , CM000681.1:g.7125449C>T	GRCh37
NC_000019.8:g.7076449C>T	NCBI36
NG_008852.2:g.173563G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3103G>A MANE Select	ENSP00000303830.4:p.Gly1035Ser
ENST00000302850.9:c.3103G>A	ENSP00000303830.4:p.Gly1035Ser
ENST00000341500.9:c.3067G>A	ENSP00000342838.4:p.Gly1023Ser
NM_000208.2:c.3103G>A	NP_000199.2:p.Gly1035Ser
NM_000208.3:c.3103G>A	NP_000199.2:p.Gly1035Ser
NM_001079817.1:c.3067G>A	NP_001073285.1:p.Gly1023Ser
NM_001079817.2:c.3067G>A	NP_001073285.1:p.Gly1023Ser
XM_011527988.1:c.3178G>A	XP_011526290.1:p.Gly1060Ser
XM_011527989.1:c.3142G>A	XP_011526291.1:p.Gly1048Ser
XM_011527988.2:c.3100G>A	XP_011526290.2:p.Gly1034Ser
XM_011527989.3:c.3064G>A	XP_011526291.2:p.Gly1022Ser
NM_000208.4:c.3103G>A MANE Select	NP_000199.2:p.Gly1035Ser
NM_001079817.3:c.3067G>A	NP_001073285.1:p.Gly1023Ser