Canonical Allele Identifier: CA403671304

Gene: INSR

Linked Data

• dbSNP Id: rs764479879
• MyVariant Identifiers: chr19:g.7125449C>A (hg19) ; chr19:g.7125438C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3103G>T MANE Select	ENSP00000303830.4:p.Gly1035Cys
ENST00000302850.9:c.3103G>T	ENSP00000303830.4:p.Gly1035Cys
ENST00000341500.9:c.3067G>T	ENSP00000342838.4:p.Gly1023Cys
NM_000208.2:c.3103G>T	NP_000199.2:p.Gly1035Cys
NM_000208.3:c.3103G>T	NP_000199.2:p.Gly1035Cys
NM_001079817.1:c.3067G>T	NP_001073285.1:p.Gly1023Cys
NM_001079817.2:c.3067G>T	NP_001073285.1:p.Gly1023Cys
XM_011527988.1:c.3178G>T	XP_011526290.1:p.Gly1060Cys
XM_011527989.1:c.3142G>T	XP_011526291.1:p.Gly1048Cys
XM_011527988.2:c.3100G>T	XP_011526290.2:p.Gly1034Cys
XM_011527989.3:c.3064G>T	XP_011526291.2:p.Gly1022Cys
NM_000208.4:c.3103G>T MANE Select	NP_000199.2:p.Gly1035Cys
NM_001079817.3:c.3067G>T	NP_001073285.1:p.Gly1023Cys