Canonical Allele Identifier: CA403671103

Gene: INSR

Linked Data

• dbSNP Id: rs1324279061
• MyVariant Identifiers: chr19:g.7125356G>C (hg19) ; chr19:g.7125345G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125345G>C , CM000681.2:g.7125345G>C	GRCh38
NC_000019.9:g.7125356G>C , CM000681.1:g.7125356G>C	GRCh37
NC_000019.8:g.7076356G>C	NCBI36
NG_008852.2:g.173656C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3196C>G MANE Select	ENSP00000303830.4:p.Arg1066Gly
ENST00000302850.9:c.3196C>G	ENSP00000303830.4:p.Arg1066Gly
ENST00000341500.9:c.3160C>G	ENSP00000342838.4:p.Arg1054Gly
ENST00000593970.1:n.42C>G
NM_000208.2:c.3196C>G	NP_000199.2:p.Arg1066Gly
NM_000208.3:c.3196C>G	NP_000199.2:p.Arg1066Gly
NM_001079817.1:c.3160C>G	NP_001073285.1:p.Arg1054Gly
NM_001079817.2:c.3160C>G	NP_001073285.1:p.Arg1054Gly
XM_011527988.1:c.3271C>G	XP_011526290.1:p.Arg1091Gly
XM_011527989.1:c.3235C>G	XP_011526291.1:p.Arg1079Gly
XM_011527988.2:c.3193C>G	XP_011526290.2:p.Arg1065Gly
XM_011527989.3:c.3157C>G	XP_011526291.2:p.Arg1053Gly
NM_000208.4:c.3196C>G MANE Select	NP_000199.2:p.Arg1066Gly
NM_001079817.3:c.3160C>G	NP_001073285.1:p.Arg1054Gly