Canonical Allele Identifier: CA304873392

Gene: INSR

Linked Data

• dbSNP Id: rs74333552
• MyVariant Identifiers: chr19:g.7125440A>T (hg19) ; chr19:g.7125429A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125429A>T , CM000681.2:g.7125429A>T	GRCh38
NC_000019.9:g.7125440A>T , CM000681.1:g.7125440A>T	GRCh37
NC_000019.8:g.7076440A>T	NCBI36
NG_008852.2:g.173572T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3112T>A MANE Select	ENSP00000303830.4:p.Tyr1038Asn
ENST00000302850.9:c.3112T>A	ENSP00000303830.4:p.Tyr1038Asn
ENST00000341500.9:c.3076T>A	ENSP00000342838.4:p.Tyr1026Asn
NM_000208.2:c.3112T>A	NP_000199.2:p.Tyr1038Asn
NM_000208.3:c.3112T>A	NP_000199.2:p.Tyr1038Asn
NM_001079817.1:c.3076T>A	NP_001073285.1:p.Tyr1026Asn
NM_001079817.2:c.3076T>A	NP_001073285.1:p.Tyr1026Asn
XM_011527988.1:c.3187T>A	XP_011526290.1:p.Tyr1063Asn
XM_011527989.1:c.3151T>A	XP_011526291.1:p.Tyr1051Asn
XM_011527988.2:c.3109T>A	XP_011526290.2:p.Tyr1037Asn
XM_011527989.3:c.3073T>A	XP_011526291.2:p.Tyr1025Asn
NM_000208.4:c.3112T>A MANE Select	NP_000199.2:p.Tyr1038Asn
NM_001079817.3:c.3076T>A	NP_001073285.1:p.Tyr1026Asn