Canonical Allele Identifier: CA9136021

Gene: INSR

Linked Data

• ClinVar Variation Id: 2981747
• ClinVar RCV Id: RCV003840329
• dbSNP Id: rs762739517
• ExAC: 19:7184560 G / A
• gnomAD v2: 19-7184560-G-A
• gnomAD v3: 19-7184549-G-A
• gnomAD v4: 19-7184549-G-A
• MyVariant Identifiers: chr19:g.7184560G>A (hg19) ; chr19:g.7184549G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184549G>A , CM000681.2:g.7184549G>A	GRCh38
NC_000019.9:g.7184560G>A , CM000681.1:g.7184560G>A	GRCh37
NC_000019.8:g.7135560G>A	NCBI36
NG_008852.2:g.114452C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.741C>T MANE Select	ENSP00000303830.4:p.Asp247=
ENST00000302850.9:c.741C>T	ENSP00000303830.4:p.Asp247=
ENST00000341500.9:c.741C>T	ENSP00000342838.4:p.Asp247=
ENST00000598216.1:n.716C>T
NM_000208.2:c.741C>T	NP_000199.2:p.Asp247=
NM_000208.3:c.741C>T	NP_000199.2:p.Asp247=
NM_001079817.1:c.741C>T	NP_001073285.1:p.Asp247=
NM_001079817.2:c.741C>T	NP_001073285.1:p.Asp247=
XM_011527988.1:c.819C>T	XP_011526290.1:p.Asp273=
XM_011527989.1:c.819C>T	XP_011526291.1:p.Asp273=
XM_011527988.2:c.741C>T	XP_011526290.2:p.Asp247=
XM_011527989.3:c.741C>T	XP_011526291.2:p.Asp247=
NM_000208.4:c.741C>T MANE Select	NP_000199.2:p.Asp247=
NM_001079817.3:c.741C>T	NP_001073285.1:p.Asp247=