Canonical Allele Identifier: CA403668498

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117210G>C (hg19) ; chr19:g.7117199G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117199G>C , CM000681.2:g.7117199G>C	GRCh38
NC_000019.9:g.7117210G>C , CM000681.1:g.7117210G>C	GRCh37
NC_000019.8:g.7068210G>C	NCBI36
NG_008852.2:g.181802C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4006C>G MANE Select	ENSP00000303830.4:p.Gln1336Glu
ENST00000302850.9:c.4006C>G	ENSP00000303830.4:p.Gln1336Glu
ENST00000341500.9:c.3970C>G	ENSP00000342838.4:p.Gln1324Glu
NM_000208.2:c.4006C>G	NP_000199.2:p.Gln1336Glu
NM_000208.3:c.4006C>G	NP_000199.2:p.Gln1336Glu
NM_001079817.1:c.3970C>G	NP_001073285.1:p.Gln1324Glu
NM_001079817.2:c.3970C>G	NP_001073285.1:p.Gln1324Glu
XM_011527988.1:c.4081C>G	XP_011526290.1:p.Gln1361Glu
XM_011527989.1:c.4045C>G	XP_011526291.1:p.Gln1349Glu
XM_011527988.2:c.4003C>G	XP_011526290.2:p.Gln1335Glu
XM_011527989.3:c.3967C>G	XP_011526291.2:p.Gln1323Glu
NM_000208.4:c.4006C>G MANE Select	NP_000199.2:p.Gln1336Glu
NM_001079817.3:c.3970C>G	NP_001073285.1:p.Gln1324Glu