Canonical Allele Identifier: CA403668250

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117096G>T (hg19) ; chr19:g.7117085G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117085G>T , CM000681.2:g.7117085G>T	GRCh38
NC_000019.9:g.7117096G>T , CM000681.1:g.7117096G>T	GRCh37
NC_000019.8:g.7068096G>T	NCBI36
NG_008852.2:g.181916C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4120C>A MANE Select	ENSP00000303830.4:p.Leu1374Met
ENST00000302850.9:c.4120C>A	ENSP00000303830.4:p.Leu1374Met
ENST00000341500.9:c.4084C>A	ENSP00000342838.4:p.Leu1362Met
NM_000208.2:c.4120C>A	NP_000199.2:p.Leu1374Met
NM_000208.3:c.4120C>A	NP_000199.2:p.Leu1374Met
NM_001079817.1:c.4084C>A	NP_001073285.1:p.Leu1362Met
NM_001079817.2:c.4084C>A	NP_001073285.1:p.Leu1362Met
XM_011527988.1:c.4195C>A	XP_011526290.1:p.Leu1399Met
XM_011527989.1:c.4159C>A	XP_011526291.1:p.Leu1387Met
XM_011527988.2:c.4117C>A	XP_011526290.2:p.Leu1373Met
XM_011527989.3:c.4081C>A	XP_011526291.2:p.Leu1361Met
NM_000208.4:c.4120C>A MANE Select	NP_000199.2:p.Leu1374Met
NM_001079817.3:c.4084C>A	NP_001073285.1:p.Leu1362Met