Canonical Allele Identifier: CA505217089

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122956C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122945C>G , CM000681.2:g.7122945C>G	GRCh38
NC_000019.9:g.7122956C>G , CM000681.1:g.7122956C>G	GRCh37
NC_000019.8:g.7073956C>G	NCBI36
NG_008852.2:g.176056G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3303G>C MANE Select	ENSP00000303830.4:p.Val1101=
ENST00000302850.9:c.3303G>C	ENSP00000303830.4:p.Val1101=
ENST00000341500.9:c.3267G>C	ENSP00000342838.4:p.Val1089=
ENST00000593970.1:n.149G>C
ENST00000601099.1:n.214G>C
NM_000208.2:c.3303G>C	NP_000199.2:p.Val1101=
NM_000208.3:c.3303G>C	NP_000199.2:p.Val1101=
NM_001079817.1:c.3267G>C	NP_001073285.1:p.Val1089=
NM_001079817.2:c.3267G>C	NP_001073285.1:p.Val1089=
XM_011527988.1:c.3378G>C	XP_011526290.1:p.Val1126=
XM_011527989.1:c.3342G>C	XP_011526291.1:p.Val1114=
XM_011527988.2:c.3300G>C	XP_011526290.2:p.Val1100=
XM_011527989.3:c.3264G>C	XP_011526291.2:p.Val1088=
NM_000208.4:c.3303G>C MANE Select	NP_000199.2:p.Val1101=
NM_001079817.3:c.3267G>C	NP_001073285.1:p.Val1089=