Canonical Allele Identifier: CA403671465

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125527A>C (hg19) ; chr19:g.7125516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125516A>C , CM000681.2:g.7125516A>C	GRCh38
NC_000019.9:g.7125527A>C , CM000681.1:g.7125527A>C	GRCh37
NC_000019.8:g.7076527A>C	NCBI36
NG_008852.2:g.173485T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3025T>G MANE Select	ENSP00000303830.4:p.Ser1009Ala
ENST00000302850.9:c.3025T>G	ENSP00000303830.4:p.Ser1009Ala
ENST00000341500.9:c.2989T>G	ENSP00000342838.4:p.Ser997Ala
NM_000208.2:c.3025T>G	NP_000199.2:p.Ser1009Ala
NM_000208.3:c.3025T>G	NP_000199.2:p.Ser1009Ala
NM_001079817.1:c.2989T>G	NP_001073285.1:p.Ser997Ala
NM_001079817.2:c.2989T>G	NP_001073285.1:p.Ser997Ala
XM_011527988.1:c.3100T>G	XP_011526290.1:p.Ser1034Ala
XM_011527989.1:c.3064T>G	XP_011526291.1:p.Ser1022Ala
XM_011527988.2:c.3022T>G	XP_011526290.2:p.Ser1008Ala
XM_011527989.3:c.2986T>G	XP_011526291.2:p.Ser996Ala
NM_000208.4:c.3025T>G MANE Select	NP_000199.2:p.Ser1009Ala
NM_001079817.3:c.2989T>G	NP_001073285.1:p.Ser997Ala