Canonical Allele Identifier: CA403668687

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117292C>G (hg19) ; chr19:g.7117281C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117281C>G , CM000681.2:g.7117281C>G	GRCh38
NC_000019.9:g.7117292C>G , CM000681.1:g.7117292C>G	GRCh37
NC_000019.8:g.7068292C>G	NCBI36
NG_008852.2:g.181720G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3924G>C MANE Select	ENSP00000303830.4:p.Glu1308Asp
ENST00000302850.9:c.3924G>C	ENSP00000303830.4:p.Glu1308Asp
ENST00000341500.9:c.3888G>C	ENSP00000342838.4:p.Glu1296Asp
NM_000208.2:c.3924G>C	NP_000199.2:p.Glu1308Asp
NM_000208.3:c.3924G>C	NP_000199.2:p.Glu1308Asp
NM_001079817.1:c.3888G>C	NP_001073285.1:p.Glu1296Asp
NM_001079817.2:c.3888G>C	NP_001073285.1:p.Glu1296Asp
XM_011527988.1:c.3999G>C	XP_011526290.1:p.Glu1333Asp
XM_011527989.1:c.3963G>C	XP_011526291.1:p.Glu1321Asp
XM_011527988.2:c.3921G>C	XP_011526290.2:p.Glu1307Asp
XM_011527989.3:c.3885G>C	XP_011526291.2:p.Glu1295Asp
NM_000208.4:c.3924G>C MANE Select	NP_000199.2:p.Glu1308Asp
NM_001079817.3:c.3888G>C	NP_001073285.1:p.Glu1296Asp