Canonical Allele Identifier: CA403668253

Gene: INSR

Linked Data

• gnomAD v4: 19-7117087-A-G
• MyVariant Identifiers: chr19:g.7117098A>G (hg19) ; chr19:g.7117087A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117087A>G , CM000681.2:g.7117087A>G	GRCh38
NC_000019.9:g.7117098A>G , CM000681.1:g.7117098A>G	GRCh37
NC_000019.8:g.7068098A>G	NCBI36
NG_008852.2:g.181914T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4118T>C MANE Select	ENSP00000303830.4:p.Ile1373Thr
ENST00000302850.9:c.4118T>C	ENSP00000303830.4:p.Ile1373Thr
ENST00000341500.9:c.4082T>C	ENSP00000342838.4:p.Ile1361Thr
NM_000208.2:c.4118T>C	NP_000199.2:p.Ile1373Thr
NM_000208.3:c.4118T>C	NP_000199.2:p.Ile1373Thr
NM_001079817.1:c.4082T>C	NP_001073285.1:p.Ile1361Thr
NM_001079817.2:c.4082T>C	NP_001073285.1:p.Ile1361Thr
XM_011527988.1:c.4193T>C	XP_011526290.1:p.Ile1398Thr
XM_011527989.1:c.4157T>C	XP_011526291.1:p.Ile1386Thr
XM_011527988.2:c.4115T>C	XP_011526290.2:p.Ile1372Thr
XM_011527989.3:c.4079T>C	XP_011526291.2:p.Ile1360Thr
NM_000208.4:c.4118T>C MANE Select	NP_000199.2:p.Ile1373Thr
NM_001079817.3:c.4082T>C	NP_001073285.1:p.Ile1361Thr