Canonical Allele Identifier: CA403668243

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117093T>C (hg19) ; chr19:g.7117082T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117082T>C , CM000681.2:g.7117082T>C	GRCh38
NC_000019.9:g.7117093T>C , CM000681.1:g.7117093T>C	GRCh37
NC_000019.8:g.7068093T>C	NCBI36
NG_008852.2:g.181919A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4123A>G MANE Select	ENSP00000303830.4:p.Thr1375Ala
ENST00000302850.9:c.4123A>G	ENSP00000303830.4:p.Thr1375Ala
ENST00000341500.9:c.4087A>G	ENSP00000342838.4:p.Thr1363Ala
NM_000208.2:c.4123A>G	NP_000199.2:p.Thr1375Ala
NM_000208.3:c.4123A>G	NP_000199.2:p.Thr1375Ala
NM_001079817.1:c.4087A>G	NP_001073285.1:p.Thr1363Ala
NM_001079817.2:c.4087A>G	NP_001073285.1:p.Thr1363Ala
XM_011527988.1:c.4198A>G	XP_011526290.1:p.Thr1400Ala
XM_011527989.1:c.4162A>G	XP_011526291.1:p.Thr1388Ala
XM_011527988.2:c.4120A>G	XP_011526290.2:p.Thr1374Ala
XM_011527989.3:c.4084A>G	XP_011526291.2:p.Thr1362Ala
NM_000208.4:c.4123A>G MANE Select	NP_000199.2:p.Thr1375Ala
NM_001079817.3:c.4087A>G	NP_001073285.1:p.Thr1363Ala