Canonical Allele Identifier: CA403671072

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125341A>C (hg19) ; chr19:g.7125330A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125330A>C , CM000681.2:g.7125330A>C	GRCh38
NC_000019.9:g.7125341A>C , CM000681.1:g.7125341A>C	GRCh37
NC_000019.8:g.7076341A>C	NCBI36
NG_008852.2:g.173671T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3211T>G MANE Select	ENSP00000303830.4:p.Phe1071Val
ENST00000302850.9:c.3211T>G	ENSP00000303830.4:p.Phe1071Val
ENST00000341500.9:c.3175T>G	ENSP00000342838.4:p.Phe1059Val
ENST00000593970.1:n.57T>G
NM_000208.2:c.3211T>G	NP_000199.2:p.Phe1071Val
NM_000208.3:c.3211T>G	NP_000199.2:p.Phe1071Val
NM_001079817.1:c.3175T>G	NP_001073285.1:p.Phe1059Val
NM_001079817.2:c.3175T>G	NP_001073285.1:p.Phe1059Val
XM_011527988.1:c.3286T>G	XP_011526290.1:p.Phe1096Val
XM_011527989.1:c.3250T>G	XP_011526291.1:p.Phe1084Val
XM_011527988.2:c.3208T>G	XP_011526290.2:p.Phe1070Val
XM_011527989.3:c.3172T>G	XP_011526291.2:p.Phe1058Val
NM_000208.4:c.3211T>G MANE Select	NP_000199.2:p.Phe1071Val
NM_001079817.3:c.3175T>G	NP_001073285.1:p.Phe1059Val