Canonical Allele Identifier: CA403668468

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117198C>G (hg19) ; chr19:g.7117187C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117187C>G , CM000681.2:g.7117187C>G	GRCh38
NC_000019.9:g.7117198C>G , CM000681.1:g.7117198C>G	GRCh37
NC_000019.8:g.7068198C>G	NCBI36
NG_008852.2:g.181814G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4018G>C MANE Select	ENSP00000303830.4:p.Ala1340Pro
ENST00000302850.9:c.4018G>C	ENSP00000303830.4:p.Ala1340Pro
ENST00000341500.9:c.3982G>C	ENSP00000342838.4:p.Ala1328Pro
NM_000208.2:c.4018G>C	NP_000199.2:p.Ala1340Pro
NM_000208.3:c.4018G>C	NP_000199.2:p.Ala1340Pro
NM_001079817.1:c.3982G>C	NP_001073285.1:p.Ala1328Pro
NM_001079817.2:c.3982G>C	NP_001073285.1:p.Ala1328Pro
XM_011527988.1:c.4093G>C	XP_011526290.1:p.Ala1365Pro
XM_011527989.1:c.4057G>C	XP_011526291.1:p.Ala1353Pro
XM_011527988.2:c.4015G>C	XP_011526290.2:p.Ala1339Pro
XM_011527989.3:c.3979G>C	XP_011526291.2:p.Ala1327Pro
NM_000208.4:c.4018G>C MANE Select	NP_000199.2:p.Ala1340Pro
NM_001079817.3:c.3982G>C	NP_001073285.1:p.Ala1328Pro