Canonical Allele Identifier: CA505400011

Gene: INSR

Linked Data

• dbSNP Id: rs1972351942
• COSMIC: COSM3541165 ; COSM3541166
• MyVariant Identifiers: chr19:g.7117139G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117128G>A , CM000681.2:g.7117128G>A	GRCh38
NC_000019.9:g.7117139G>A , CM000681.1:g.7117139G>A	GRCh37
NC_000019.8:g.7068139G>A	NCBI36
NG_008852.2:g.181873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4077C>T MANE Select	ENSP00000303830.4:p.Ile1359=
ENST00000302850.9:c.4077C>T	ENSP00000303830.4:p.Ile1359=
ENST00000341500.9:c.4041C>T	ENSP00000342838.4:p.Ile1347=
NM_000208.2:c.4077C>T	NP_000199.2:p.Ile1359=
NM_000208.3:c.4077C>T	NP_000199.2:p.Ile1359=
NM_001079817.1:c.4041C>T	NP_001073285.1:p.Ile1347=
NM_001079817.2:c.4041C>T	NP_001073285.1:p.Ile1347=
XM_011527988.1:c.4152C>T	XP_011526290.1:p.Ile1384=
XM_011527989.1:c.4116C>T	XP_011526291.1:p.Ile1372=
XM_011527988.2:c.4074C>T	XP_011526290.2:p.Ile1358=
XM_011527989.3:c.4038C>T	XP_011526291.2:p.Ile1346=
NM_000208.4:c.4077C>T MANE Select	NP_000199.2:p.Ile1359=
NM_001079817.3:c.4041C>T	NP_001073285.1:p.Ile1347=