Canonical Allele Identifier: CA505400126

Gene: INSR

Linked Data

• dbSNP Id: rs1227200864
• gnomAD v2: 19-7117349-C-T
• gnomAD v3: 19-7117338-C-T
• gnomAD v4: 19-7117338-C-T
• MyVariant Identifiers: chr19:g.7117349C>T (hg19) ; chr19:g.7117338C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117338C>T , CM000681.2:g.7117338C>T	GRCh38
NC_000019.9:g.7117349C>T , CM000681.1:g.7117349C>T	GRCh37
NC_000019.8:g.7068349C>T	NCBI36
NG_008852.2:g.181663G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3867G>A MANE Select	ENSP00000303830.4:p.Leu1289=
ENST00000302850.9:c.3867G>A	ENSP00000303830.4:p.Leu1289=
ENST00000341500.9:c.3831G>A	ENSP00000342838.4:p.Leu1277=
NM_000208.2:c.3867G>A	NP_000199.2:p.Leu1289=
NM_000208.3:c.3867G>A	NP_000199.2:p.Leu1289=
NM_001079817.1:c.3831G>A	NP_001073285.1:p.Leu1277=
NM_001079817.2:c.3831G>A	NP_001073285.1:p.Leu1277=
XM_011527988.1:c.3942G>A	XP_011526290.1:p.Leu1314=
XM_011527989.1:c.3906G>A	XP_011526291.1:p.Leu1302=
XM_011527988.2:c.3864G>A	XP_011526290.2:p.Leu1288=
XM_011527989.3:c.3828G>A	XP_011526291.2:p.Leu1276=
NM_000208.4:c.3867G>A MANE Select	NP_000199.2:p.Leu1289=
NM_001079817.3:c.3831G>A	NP_001073285.1:p.Leu1277=