Canonical Allele Identifier: CA403672058

Gene: INSR

Linked Data

• ClinVar Variation Id: 2335283
• ClinVar RCV Id: RCV002921673
• MyVariant Identifiers: chr19:g.7132246C>T (hg19) ; chr19:g.7132235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132235C>T , CM000681.2:g.7132235C>T	GRCh38
NC_000019.9:g.7132246C>T , CM000681.1:g.7132246C>T	GRCh37
NC_000019.8:g.7083246C>T	NCBI36
NG_008852.2:g.166766G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2765G>A MANE Select	ENSP00000303830.4:p.Ser922Asn
ENST00000302850.9:c.2765G>A	ENSP00000303830.4:p.Ser922Asn
ENST00000341500.9:c.2729G>A	ENSP00000342838.4:p.Ser910Asn
NM_000208.2:c.2765G>A	NP_000199.2:p.Ser922Asn
NM_000208.3:c.2765G>A	NP_000199.2:p.Ser922Asn
NM_001079817.1:c.2729G>A	NP_001073285.1:p.Ser910Asn
NM_001079817.2:c.2729G>A	NP_001073285.1:p.Ser910Asn
XM_011527988.1:c.2843G>A	XP_011526290.1:p.Ser948Asn
XM_011527989.1:c.2807G>A	XP_011526291.1:p.Ser936Asn
XM_011527988.2:c.2765G>A	XP_011526290.2:p.Ser922Asn
XM_011527989.3:c.2729G>A	XP_011526291.2:p.Ser910Asn
NM_000208.4:c.2765G>A MANE Select	NP_000199.2:p.Ser922Asn
NM_001079817.3:c.2729G>A	NP_001073285.1:p.Ser910Asn