Canonical Allele Identifier: CA403668259

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117101C>G (hg19) ; chr19:g.7117090C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117090C>G , CM000681.2:g.7117090C>G	GRCh38
NC_000019.9:g.7117101C>G , CM000681.1:g.7117101C>G	GRCh37
NC_000019.8:g.7068101C>G	NCBI36
NG_008852.2:g.181911G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4115G>C MANE Select	ENSP00000303830.4:p.Arg1372Pro
ENST00000302850.9:c.4115G>C	ENSP00000303830.4:p.Arg1372Pro
ENST00000341500.9:c.4079G>C	ENSP00000342838.4:p.Arg1360Pro
NM_000208.2:c.4115G>C	NP_000199.2:p.Arg1372Pro
NM_000208.3:c.4115G>C	NP_000199.2:p.Arg1372Pro
NM_001079817.1:c.4079G>C	NP_001073285.1:p.Arg1360Pro
NM_001079817.2:c.4079G>C	NP_001073285.1:p.Arg1360Pro
XM_011527988.1:c.4190G>C	XP_011526290.1:p.Arg1397Pro
XM_011527989.1:c.4154G>C	XP_011526291.1:p.Arg1385Pro
XM_011527988.2:c.4112G>C	XP_011526290.2:p.Arg1371Pro
XM_011527989.3:c.4076G>C	XP_011526291.2:p.Arg1359Pro
NM_000208.4:c.4115G>C MANE Select	NP_000199.2:p.Arg1372Pro
NM_001079817.3:c.4079G>C	NP_001073285.1:p.Arg1360Pro