Canonical Allele Identifier: CA505400446

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7143086G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7143075G>C , CM000681.2:g.7143075G>C	GRCh38
NC_000019.9:g.7143086G>C , CM000681.1:g.7143086G>C	GRCh37
NC_000019.8:g.7094086G>C	NCBI36
NG_008852.2:g.155926C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2283C>G MANE Select	ENSP00000303830.4:p.Arg761=
ENST00000302850.9:c.2283C>G	ENSP00000303830.4:p.Arg761=
ENST00000341500.9:c.2247C>G	ENSP00000342838.4:p.Arg749=
NM_000208.2:c.2283C>G	NP_000199.2:p.Arg761=
NM_000208.3:c.2283C>G	NP_000199.2:p.Arg761=
NM_001079817.1:c.2247C>G	NP_001073285.1:p.Arg749=
NM_001079817.2:c.2247C>G	NP_001073285.1:p.Arg749=
XM_011527988.1:c.2361C>G	XP_011526290.1:p.Arg787=
XM_011527989.1:c.2325C>G	XP_011526291.1:p.Arg775=
XM_011527988.2:c.2283C>G	XP_011526290.2:p.Arg761=
XM_011527989.3:c.2247C>G	XP_011526291.2:p.Arg749=
NM_000208.4:c.2283C>G MANE Select	NP_000199.2:p.Arg761=
NM_001079817.3:c.2247C>G	NP_001073285.1:p.Arg749=