Canonical Allele Identifier: CA304866570

Gene: INSR

Linked Data

• dbSNP Id: rs772180057
• gnomAD v4: 19-7117282-T-A
• MyVariant Identifiers: chr19:g.7117293T>A (hg19) ; chr19:g.7117282T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117282T>A , CM000681.2:g.7117282T>A	GRCh38
NC_000019.9:g.7117293T>A , CM000681.1:g.7117293T>A	GRCh37
NC_000019.8:g.7068293T>A	NCBI36
NG_008852.2:g.181719A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3923A>T MANE Select	ENSP00000303830.4:p.Glu1308Val
ENST00000302850.9:c.3923A>T	ENSP00000303830.4:p.Glu1308Val
ENST00000341500.9:c.3887A>T	ENSP00000342838.4:p.Glu1296Val
NM_000208.2:c.3923A>T	NP_000199.2:p.Glu1308Val
NM_000208.3:c.3923A>T	NP_000199.2:p.Glu1308Val
NM_001079817.1:c.3887A>T	NP_001073285.1:p.Glu1296Val
NM_001079817.2:c.3887A>T	NP_001073285.1:p.Glu1296Val
XM_011527988.1:c.3998A>T	XP_011526290.1:p.Glu1333Val
XM_011527989.1:c.3962A>T	XP_011526291.1:p.Glu1321Val
XM_011527988.2:c.3920A>T	XP_011526290.2:p.Glu1307Val
XM_011527989.3:c.3884A>T	XP_011526291.2:p.Glu1295Val
NM_000208.4:c.3923A>T MANE Select	NP_000199.2:p.Glu1308Val
NM_001079817.3:c.3887A>T	NP_001073285.1:p.Glu1296Val