Canonical Allele Identifier: CA403668510

Gene: INSR

Linked Data

• gnomAD v4: 19-7117204-T-C
• MyVariant Identifiers: chr19:g.7117215T>C (hg19) ; chr19:g.7117204T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117204T>C , CM000681.2:g.7117204T>C	GRCh38
NC_000019.9:g.7117215T>C , CM000681.1:g.7117215T>C	GRCh37
NC_000019.8:g.7068215T>C	NCBI36
NG_008852.2:g.181797A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4001A>G MANE Select	ENSP00000303830.4:p.His1334Arg
ENST00000302850.9:c.4001A>G	ENSP00000303830.4:p.His1334Arg
ENST00000341500.9:c.3965A>G	ENSP00000342838.4:p.His1322Arg
NM_000208.2:c.4001A>G	NP_000199.2:p.His1334Arg
NM_000208.3:c.4001A>G	NP_000199.2:p.His1334Arg
NM_001079817.1:c.3965A>G	NP_001073285.1:p.His1322Arg
NM_001079817.2:c.3965A>G	NP_001073285.1:p.His1322Arg
XM_011527988.1:c.4076A>G	XP_011526290.1:p.His1359Arg
XM_011527989.1:c.4040A>G	XP_011526291.1:p.His1347Arg
XM_011527988.2:c.3998A>G	XP_011526290.2:p.His1333Arg
XM_011527989.3:c.3962A>G	XP_011526291.2:p.His1321Arg
NM_000208.4:c.4001A>G MANE Select	NP_000199.2:p.His1334Arg
NM_001079817.3:c.3965A>G	NP_001073285.1:p.His1322Arg