Canonical Allele Identifier: CA403672119

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132276C>T (hg19) ; chr19:g.7132265C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132265C>T , CM000681.2:g.7132265C>T	GRCh38
NC_000019.9:g.7132276C>T , CM000681.1:g.7132276C>T	GRCh37
NC_000019.8:g.7083276C>T	NCBI36
NG_008852.2:g.166736G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2735G>A MANE Select	ENSP00000303830.4:p.Arg912Lys
ENST00000302850.9:c.2735G>A	ENSP00000303830.4:p.Arg912Lys
ENST00000341500.9:c.2699G>A	ENSP00000342838.4:p.Arg900Lys
NM_000208.2:c.2735G>A	NP_000199.2:p.Arg912Lys
NM_000208.3:c.2735G>A	NP_000199.2:p.Arg912Lys
NM_001079817.1:c.2699G>A	NP_001073285.1:p.Arg900Lys
NM_001079817.2:c.2699G>A	NP_001073285.1:p.Arg900Lys
XM_011527988.1:c.2813G>A	XP_011526290.1:p.Arg938Lys
XM_011527989.1:c.2777G>A	XP_011526291.1:p.Arg926Lys
XM_011527988.2:c.2735G>A	XP_011526290.2:p.Arg912Lys
XM_011527989.3:c.2699G>A	XP_011526291.2:p.Arg900Lys
NM_000208.4:c.2735G>A MANE Select	NP_000199.2:p.Arg912Lys
NM_001079817.3:c.2699G>A	NP_001073285.1:p.Arg900Lys