Canonical Allele Identifier: CA505400049

Gene: INSR

Linked Data

• gnomAD v4: 19-7117182-C-A
• MyVariant Identifiers: chr19:g.7117193C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117182C>A , CM000681.2:g.7117182C>A	GRCh38
NC_000019.9:g.7117193C>A , CM000681.1:g.7117193C>A	GRCh37
NC_000019.8:g.7068193C>A	NCBI36
NG_008852.2:g.181819G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4023G>T MANE Select	ENSP00000303830.4:p.Gly1341=
ENST00000302850.9:c.4023G>T	ENSP00000303830.4:p.Gly1341=
ENST00000341500.9:c.3987G>T	ENSP00000342838.4:p.Gly1329=
NM_000208.2:c.4023G>T	NP_000199.2:p.Gly1341=
NM_000208.3:c.4023G>T	NP_000199.2:p.Gly1341=
NM_001079817.1:c.3987G>T	NP_001073285.1:p.Gly1329=
NM_001079817.2:c.3987G>T	NP_001073285.1:p.Gly1329=
XM_011527988.1:c.4098G>T	XP_011526290.1:p.Gly1366=
XM_011527989.1:c.4062G>T	XP_011526291.1:p.Gly1354=
XM_011527988.2:c.4020G>T	XP_011526290.2:p.Gly1340=
XM_011527989.3:c.3984G>T	XP_011526291.2:p.Gly1328=
NM_000208.4:c.4023G>T MANE Select	NP_000199.2:p.Gly1341=
NM_001079817.3:c.3987G>T	NP_001073285.1:p.Gly1329=