Canonical Allele Identifier: CA505217687

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132317G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132306G>C , CM000681.2:g.7132306G>C	GRCh38
NC_000019.9:g.7132317G>C , CM000681.1:g.7132317G>C	GRCh37
NC_000019.8:g.7083317G>C	NCBI36
NG_008852.2:g.166695C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2694C>G MANE Select	ENSP00000303830.4:p.Leu898=
ENST00000302850.9:c.2694C>G	ENSP00000303830.4:p.Leu898=
ENST00000341500.9:c.2658C>G	ENSP00000342838.4:p.Leu886=
NM_000208.2:c.2694C>G	NP_000199.2:p.Leu898=
NM_000208.3:c.2694C>G	NP_000199.2:p.Leu898=
NM_001079817.1:c.2658C>G	NP_001073285.1:p.Leu886=
NM_001079817.2:c.2658C>G	NP_001073285.1:p.Leu886=
XM_011527988.1:c.2772C>G	XP_011526290.1:p.Leu924=
XM_011527989.1:c.2736C>G	XP_011526291.1:p.Leu912=
XM_011527988.2:c.2694C>G	XP_011526290.2:p.Leu898=
XM_011527989.3:c.2658C>G	XP_011526291.2:p.Leu886=
NM_000208.4:c.2694C>G MANE Select	NP_000199.2:p.Leu898=
NM_001079817.3:c.2658C>G	NP_001073285.1:p.Leu886=