Canonical Allele Identifier: CA304876008

Gene: INSR

Linked Data

• dbSNP Id: rs897199307
• MyVariant Identifiers: chr19:g.7128896A>G (hg19) ; chr19:g.7128885A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128885A>G , CM000681.2:g.7128885A>G	GRCh38
NC_000019.9:g.7128896A>G , CM000681.1:g.7128896A>G	GRCh37
NC_000019.8:g.7079896A>G	NCBI36
NG_008852.2:g.170116T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2912T>C MANE Select	ENSP00000303830.4:p.Val971Ala
ENST00000302850.9:c.2912T>C	ENSP00000303830.4:p.Val971Ala
ENST00000341500.9:c.2876T>C	ENSP00000342838.4:p.Val959Ala
NM_000208.2:c.2912T>C	NP_000199.2:p.Val971Ala
NM_000208.3:c.2912T>C	NP_000199.2:p.Val971Ala
NM_001079817.1:c.2876T>C	NP_001073285.1:p.Val959Ala
NM_001079817.2:c.2876T>C	NP_001073285.1:p.Val959Ala
XM_011527988.1:c.2987T>C	XP_011526290.1:p.Val996Ala
XM_011527989.1:c.2951T>C	XP_011526291.1:p.Val984Ala
XM_011527988.2:c.2909T>C	XP_011526290.2:p.Val970Ala
XM_011527989.3:c.2873T>C	XP_011526291.2:p.Val958Ala
NM_000208.4:c.2912T>C MANE Select	NP_000199.2:p.Val971Ala
NM_001079817.3:c.2876T>C	NP_001073285.1:p.Val959Ala