Canonical Allele Identifier: CA403668856

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117367G>C (hg19) ; chr19:g.7117356G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117356G>C , CM000681.2:g.7117356G>C	GRCh38
NC_000019.9:g.7117367G>C , CM000681.1:g.7117367G>C	GRCh37
NC_000019.8:g.7068367G>C	NCBI36
NG_008852.2:g.181645C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3849C>G MANE Select	ENSP00000303830.4:p.Phe1283Leu
ENST00000302850.9:c.3849C>G	ENSP00000303830.4:p.Phe1283Leu
ENST00000341500.9:c.3813C>G	ENSP00000342838.4:p.Phe1271Leu
NM_000208.2:c.3849C>G	NP_000199.2:p.Phe1283Leu
NM_000208.3:c.3849C>G	NP_000199.2:p.Phe1283Leu
NM_001079817.1:c.3813C>G	NP_001073285.1:p.Phe1271Leu
NM_001079817.2:c.3813C>G	NP_001073285.1:p.Phe1271Leu
XM_011527988.1:c.3924C>G	XP_011526290.1:p.Phe1308Leu
XM_011527989.1:c.3888C>G	XP_011526291.1:p.Phe1296Leu
XM_011527988.2:c.3846C>G	XP_011526290.2:p.Phe1282Leu
XM_011527989.3:c.3810C>G	XP_011526291.2:p.Phe1270Leu
NM_000208.4:c.3849C>G MANE Select	NP_000199.2:p.Phe1283Leu
NM_001079817.3:c.3813C>G	NP_001073285.1:p.Phe1271Leu