Canonical Allele Identifier: CA403668337

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117135A>C (hg19) ; chr19:g.7117124A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117124A>C , CM000681.2:g.7117124A>C	GRCh38
NC_000019.9:g.7117135A>C , CM000681.1:g.7117135A>C	GRCh37
NC_000019.8:g.7068135A>C	NCBI36
NG_008852.2:g.181877T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4081T>G MANE Select	ENSP00000303830.4:p.Tyr1361Asp
ENST00000302850.9:c.4081T>G	ENSP00000303830.4:p.Tyr1361Asp
ENST00000341500.9:c.4045T>G	ENSP00000342838.4:p.Tyr1349Asp
NM_000208.2:c.4081T>G	NP_000199.2:p.Tyr1361Asp
NM_000208.3:c.4081T>G	NP_000199.2:p.Tyr1361Asp
NM_001079817.1:c.4045T>G	NP_001073285.1:p.Tyr1349Asp
NM_001079817.2:c.4045T>G	NP_001073285.1:p.Tyr1349Asp
XM_011527988.1:c.4156T>G	XP_011526290.1:p.Tyr1386Asp
XM_011527989.1:c.4120T>G	XP_011526291.1:p.Tyr1374Asp
XM_011527988.2:c.4078T>G	XP_011526290.2:p.Tyr1360Asp
XM_011527989.3:c.4042T>G	XP_011526291.2:p.Tyr1348Asp
NM_000208.4:c.4081T>G MANE Select	NP_000199.2:p.Tyr1361Asp
NM_001079817.3:c.4045T>G	NP_001073285.1:p.Tyr1349Asp