Canonical Allele Identifier: CA505199262

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7166283C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166272C>G , CM000681.2:g.7166272C>G	GRCh38
NC_000019.9:g.7166283C>G , CM000681.1:g.7166283C>G	GRCh37
NC_000019.8:g.7117283C>G	NCBI36
NG_008852.2:g.132729G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1743G>C MANE Select	ENSP00000303830.4:p.Arg581=
ENST00000302850.9:c.1743G>C	ENSP00000303830.4:p.Arg581=
ENST00000341500.9:c.1743G>C	ENSP00000342838.4:p.Arg581=
ENST00000598216.1:n.1718G>C
ENST00000600492.1:c.144G>C	ENSP00000473170.1:p.Arg48=
NM_000208.2:c.1743G>C	NP_000199.2:p.Arg581=
NM_000208.3:c.1743G>C	NP_000199.2:p.Arg581=
NM_001079817.1:c.1743G>C	NP_001073285.1:p.Arg581=
NM_001079817.2:c.1743G>C	NP_001073285.1:p.Arg581=
XM_011527988.1:c.1821G>C	XP_011526290.1:p.Arg607=
XM_011527989.1:c.1821G>C	XP_011526291.1:p.Arg607=
XM_011527988.2:c.1743G>C	XP_011526290.2:p.Arg581=
XM_011527989.3:c.1743G>C	XP_011526291.2:p.Arg581=
NM_000208.4:c.1743G>C MANE Select	NP_000199.2:p.Arg581=
NM_001079817.3:c.1743G>C	NP_001073285.1:p.Arg581=