Canonical Allele Identifier: CA403668345

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117138G>T (hg19) ; chr19:g.7117127G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117127G>T , CM000681.2:g.7117127G>T	GRCh38
NC_000019.9:g.7117138G>T , CM000681.1:g.7117138G>T	GRCh37
NC_000019.8:g.7068138G>T	NCBI36
NG_008852.2:g.181874C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4078C>A MANE Select	ENSP00000303830.4:p.Pro1360Thr
ENST00000302850.9:c.4078C>A	ENSP00000303830.4:p.Pro1360Thr
ENST00000341500.9:c.4042C>A	ENSP00000342838.4:p.Pro1348Thr
NM_000208.2:c.4078C>A	NP_000199.2:p.Pro1360Thr
NM_000208.3:c.4078C>A	NP_000199.2:p.Pro1360Thr
NM_001079817.1:c.4042C>A	NP_001073285.1:p.Pro1348Thr
NM_001079817.2:c.4042C>A	NP_001073285.1:p.Pro1348Thr
XM_011527988.1:c.4153C>A	XP_011526290.1:p.Pro1385Thr
XM_011527989.1:c.4117C>A	XP_011526291.1:p.Pro1373Thr
XM_011527988.2:c.4075C>A	XP_011526290.2:p.Pro1359Thr
XM_011527989.3:c.4039C>A	XP_011526291.2:p.Pro1347Thr
NM_000208.4:c.4078C>A MANE Select	NP_000199.2:p.Pro1360Thr
NM_001079817.3:c.4042C>A	NP_001073285.1:p.Pro1348Thr