Canonical Allele Identifier: CA505216681

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120693A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120682A>T , CM000681.2:g.7120682A>T	GRCh38
NC_000019.9:g.7120693A>T , CM000681.1:g.7120693A>T	GRCh37
NC_000019.8:g.7071693A>T	NCBI36
NG_008852.2:g.178319T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3597T>A MANE Select	ENSP00000303830.4:p.Pro1199=
ENST00000302850.9:c.3597T>A	ENSP00000303830.4:p.Pro1199=
ENST00000341500.9:c.3561T>A	ENSP00000342838.4:p.Pro1187=
ENST00000601099.1:n.508T>A
NM_000208.2:c.3597T>A	NP_000199.2:p.Pro1199=
NM_000208.3:c.3597T>A	NP_000199.2:p.Pro1199=
NM_001079817.1:c.3561T>A	NP_001073285.1:p.Pro1187=
NM_001079817.2:c.3561T>A	NP_001073285.1:p.Pro1187=
XM_011527988.1:c.3672T>A	XP_011526290.1:p.Pro1224=
XM_011527989.1:c.3636T>A	XP_011526291.1:p.Pro1212=
XM_011527988.2:c.3594T>A	XP_011526290.2:p.Pro1198=
XM_011527989.3:c.3558T>A	XP_011526291.2:p.Pro1186=
NM_000208.4:c.3597T>A MANE Select	NP_000199.2:p.Pro1199=
NM_001079817.3:c.3561T>A	NP_001073285.1:p.Pro1187=