Canonical Allele Identifier: CA403668460

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117194C>A (hg19) ; chr19:g.7117183C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117183C>A , CM000681.2:g.7117183C>A	GRCh38
NC_000019.9:g.7117194C>A , CM000681.1:g.7117194C>A	GRCh37
NC_000019.8:g.7068194C>A	NCBI36
NG_008852.2:g.181818G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4022G>T MANE Select	ENSP00000303830.4:p.Gly1341Val
ENST00000302850.9:c.4022G>T	ENSP00000303830.4:p.Gly1341Val
ENST00000341500.9:c.3986G>T	ENSP00000342838.4:p.Gly1329Val
NM_000208.2:c.4022G>T	NP_000199.2:p.Gly1341Val
NM_000208.3:c.4022G>T	NP_000199.2:p.Gly1341Val
NM_001079817.1:c.3986G>T	NP_001073285.1:p.Gly1329Val
NM_001079817.2:c.3986G>T	NP_001073285.1:p.Gly1329Val
XM_011527988.1:c.4097G>T	XP_011526290.1:p.Gly1366Val
XM_011527989.1:c.4061G>T	XP_011526291.1:p.Gly1354Val
XM_011527988.2:c.4019G>T	XP_011526290.2:p.Gly1340Val
XM_011527989.3:c.3983G>T	XP_011526291.2:p.Gly1328Val
NM_000208.4:c.4022G>T MANE Select	NP_000199.2:p.Gly1341Val
NM_001079817.3:c.3986G>T	NP_001073285.1:p.Gly1329Val