Canonical Allele Identifier: CA403668228

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117086G>T (hg19) ; chr19:g.7117075G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117075G>T , CM000681.2:g.7117075G>T	GRCh38
NC_000019.9:g.7117086G>T , CM000681.1:g.7117086G>T	GRCh37
NC_000019.8:g.7068086G>T	NCBI36
NG_008852.2:g.181926C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4130C>A MANE Select	ENSP00000303830.4:p.Pro1377His
ENST00000302850.9:c.4130C>A	ENSP00000303830.4:p.Pro1377His
ENST00000341500.9:c.4094C>A	ENSP00000342838.4:p.Pro1365His
NM_000208.2:c.4130C>A	NP_000199.2:p.Pro1377His
NM_000208.3:c.4130C>A	NP_000199.2:p.Pro1377His
NM_001079817.1:c.4094C>A	NP_001073285.1:p.Pro1365His
NM_001079817.2:c.4094C>A	NP_001073285.1:p.Pro1365His
XM_011527988.1:c.4205C>A	XP_011526290.1:p.Pro1402His
XM_011527989.1:c.4169C>A	XP_011526291.1:p.Pro1390His
XM_011527988.2:c.4127C>A	XP_011526290.2:p.Pro1376His
XM_011527989.3:c.4091C>A	XP_011526291.2:p.Pro1364His
NM_000208.4:c.4130C>A MANE Select	NP_000199.2:p.Pro1377His
NM_001079817.3:c.4094C>A	NP_001073285.1:p.Pro1365His