Canonical Allele Identifier: CA505400196

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125354T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125343T>A , CM000681.2:g.7125343T>A	GRCh38
NC_000019.9:g.7125354T>A , CM000681.1:g.7125354T>A	GRCh37
NC_000019.8:g.7076354T>A	NCBI36
NG_008852.2:g.173658A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3198A>T MANE Select	ENSP00000303830.4:p.Arg1066=
ENST00000302850.9:c.3198A>T	ENSP00000303830.4:p.Arg1066=
ENST00000341500.9:c.3162A>T	ENSP00000342838.4:p.Arg1054=
ENST00000593970.1:n.44A>T
NM_000208.2:c.3198A>T	NP_000199.2:p.Arg1066=
NM_000208.3:c.3198A>T	NP_000199.2:p.Arg1066=
NM_001079817.1:c.3162A>T	NP_001073285.1:p.Arg1054=
NM_001079817.2:c.3162A>T	NP_001073285.1:p.Arg1054=
XM_011527988.1:c.3273A>T	XP_011526290.1:p.Arg1091=
XM_011527989.1:c.3237A>T	XP_011526291.1:p.Arg1079=
XM_011527988.2:c.3195A>T	XP_011526290.2:p.Arg1065=
XM_011527989.3:c.3159A>T	XP_011526291.2:p.Arg1053=
NM_000208.4:c.3198A>T MANE Select	NP_000199.2:p.Arg1066=
NM_001079817.3:c.3162A>T	NP_001073285.1:p.Arg1054=