Canonical Allele Identifier: CA403669297

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7119592G>T (hg19) ; chr19:g.7119581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119581G>T , CM000681.2:g.7119581G>T	GRCh38
NC_000019.9:g.7119592G>T , CM000681.1:g.7119592G>T	GRCh37
NC_000019.8:g.7070592G>T	NCBI36
NG_008852.2:g.179420C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3662C>A MANE Select	ENSP00000303830.4:p.Ser1221Tyr
ENST00000302850.9:c.3662C>A	ENSP00000303830.4:p.Ser1221Tyr
ENST00000341500.9:c.3626C>A	ENSP00000342838.4:p.Ser1209Tyr
NM_000208.2:c.3662C>A	NP_000199.2:p.Ser1221Tyr
NM_000208.3:c.3662C>A	NP_000199.2:p.Ser1221Tyr
NM_001079817.1:c.3626C>A	NP_001073285.1:p.Ser1209Tyr
NM_001079817.2:c.3626C>A	NP_001073285.1:p.Ser1209Tyr
XM_011527988.1:c.3737C>A	XP_011526290.1:p.Ser1246Tyr
XM_011527989.1:c.3701C>A	XP_011526291.1:p.Ser1234Tyr
XM_011527988.2:c.3659C>A	XP_011526290.2:p.Ser1220Tyr
XM_011527989.3:c.3623C>A	XP_011526291.2:p.Ser1208Tyr
NM_000208.4:c.3662C>A MANE Select	NP_000199.2:p.Ser1221Tyr
NM_001079817.3:c.3626C>A	NP_001073285.1:p.Ser1209Tyr