Canonical Allele Identifier: CA403668535

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117228C>A (hg19) ; chr19:g.7117217C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117217C>A , CM000681.2:g.7117217C>A	GRCh38
NC_000019.9:g.7117228C>A , CM000681.1:g.7117228C>A	GRCh37
NC_000019.8:g.7068228C>A	NCBI36
NG_008852.2:g.181784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3988G>T MANE Select	ENSP00000303830.4:p.Asp1330Tyr
ENST00000302850.9:c.3988G>T	ENSP00000303830.4:p.Asp1330Tyr
ENST00000341500.9:c.3952G>T	ENSP00000342838.4:p.Asp1318Tyr
NM_000208.2:c.3988G>T	NP_000199.2:p.Asp1330Tyr
NM_000208.3:c.3988G>T	NP_000199.2:p.Asp1330Tyr
NM_001079817.1:c.3952G>T	NP_001073285.1:p.Asp1318Tyr
NM_001079817.2:c.3952G>T	NP_001073285.1:p.Asp1318Tyr
XM_011527988.1:c.4063G>T	XP_011526290.1:p.Asp1355Tyr
XM_011527989.1:c.4027G>T	XP_011526291.1:p.Asp1343Tyr
XM_011527988.2:c.3985G>T	XP_011526290.2:p.Asp1329Tyr
XM_011527989.3:c.3949G>T	XP_011526291.2:p.Asp1317Tyr
NM_000208.4:c.3988G>T MANE Select	NP_000199.2:p.Asp1330Tyr
NM_001079817.3:c.3952G>T	NP_001073285.1:p.Asp1318Tyr