Canonical Allele Identifier: CA403672138

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132286G>C (hg19) ; chr19:g.7132275G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132275G>C , CM000681.2:g.7132275G>C	GRCh38
NC_000019.9:g.7132286G>C , CM000681.1:g.7132286G>C	GRCh37
NC_000019.8:g.7083286G>C	NCBI36
NG_008852.2:g.166726C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2725C>G MANE Select	ENSP00000303830.4:p.Arg909Gly
ENST00000302850.9:c.2725C>G	ENSP00000303830.4:p.Arg909Gly
ENST00000341500.9:c.2689C>G	ENSP00000342838.4:p.Arg897Gly
NM_000208.2:c.2725C>G	NP_000199.2:p.Arg909Gly
NM_000208.3:c.2725C>G	NP_000199.2:p.Arg909Gly
NM_001079817.1:c.2689C>G	NP_001073285.1:p.Arg897Gly
NM_001079817.2:c.2689C>G	NP_001073285.1:p.Arg897Gly
XM_011527988.1:c.2803C>G	XP_011526290.1:p.Arg935Gly
XM_011527989.1:c.2767C>G	XP_011526291.1:p.Arg923Gly
XM_011527988.2:c.2725C>G	XP_011526290.2:p.Arg909Gly
XM_011527989.3:c.2689C>G	XP_011526291.2:p.Arg897Gly
NM_000208.4:c.2725C>G MANE Select	NP_000199.2:p.Arg909Gly
NM_001079817.3:c.2689C>G	NP_001073285.1:p.Arg897Gly