Canonical Allele Identifier: CA403672050

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132243A>G (hg19) ; chr19:g.7132232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132232A>G , CM000681.2:g.7132232A>G	GRCh38
NC_000019.9:g.7132243A>G , CM000681.1:g.7132243A>G	GRCh37
NC_000019.8:g.7083243A>G	NCBI36
NG_008852.2:g.166769T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2768T>C MANE Select	ENSP00000303830.4:p.Val923Ala
ENST00000302850.9:c.2768T>C	ENSP00000303830.4:p.Val923Ala
ENST00000341500.9:c.2732T>C	ENSP00000342838.4:p.Val911Ala
NM_000208.2:c.2768T>C	NP_000199.2:p.Val923Ala
NM_000208.3:c.2768T>C	NP_000199.2:p.Val923Ala
NM_001079817.1:c.2732T>C	NP_001073285.1:p.Val911Ala
NM_001079817.2:c.2732T>C	NP_001073285.1:p.Val911Ala
XM_011527988.1:c.2846T>C	XP_011526290.1:p.Val949Ala
XM_011527989.1:c.2810T>C	XP_011526291.1:p.Val937Ala
XM_011527988.2:c.2768T>C	XP_011526290.2:p.Val923Ala
XM_011527989.3:c.2732T>C	XP_011526291.2:p.Val911Ala
NM_000208.4:c.2768T>C MANE Select	NP_000199.2:p.Val923Ala
NM_001079817.3:c.2732T>C	NP_001073285.1:p.Val911Ala