Canonical Allele Identifier: CA505400267

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125471T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125460T>G , CM000681.2:g.7125460T>G	GRCh38
NC_000019.9:g.7125471T>G , CM000681.1:g.7125471T>G	GRCh37
NC_000019.8:g.7076471T>G	NCBI36
NG_008852.2:g.173541A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3081A>C MANE Select	ENSP00000303830.4:p.Arg1027=
ENST00000302850.9:c.3081A>C	ENSP00000303830.4:p.Arg1027=
ENST00000341500.9:c.3045A>C	ENSP00000342838.4:p.Arg1015=
NM_000208.2:c.3081A>C	NP_000199.2:p.Arg1027=
NM_000208.3:c.3081A>C	NP_000199.2:p.Arg1027=
NM_001079817.1:c.3045A>C	NP_001073285.1:p.Arg1015=
NM_001079817.2:c.3045A>C	NP_001073285.1:p.Arg1015=
XM_011527988.1:c.3156A>C	XP_011526290.1:p.Arg1052=
XM_011527989.1:c.3120A>C	XP_011526291.1:p.Arg1040=
XM_011527988.2:c.3078A>C	XP_011526290.2:p.Arg1026=
XM_011527989.3:c.3042A>C	XP_011526291.2:p.Arg1014=
NM_000208.4:c.3081A>C MANE Select	NP_000199.2:p.Arg1027=
NM_001079817.3:c.3045A>C	NP_001073285.1:p.Arg1015=