Canonical Allele Identifier: CA403668558

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117239T>G (hg19) ; chr19:g.7117228T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117228T>G , CM000681.2:g.7117228T>G	GRCh38
NC_000019.9:g.7117239T>G , CM000681.1:g.7117239T>G	GRCh37
NC_000019.8:g.7068239T>G	NCBI36
NG_008852.2:g.181773A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3977A>C MANE Select	ENSP00000303830.4:p.Asn1326Thr
ENST00000302850.9:c.3977A>C	ENSP00000303830.4:p.Asn1326Thr
ENST00000341500.9:c.3941A>C	ENSP00000342838.4:p.Asn1314Thr
NM_000208.2:c.3977A>C	NP_000199.2:p.Asn1326Thr
NM_000208.3:c.3977A>C	NP_000199.2:p.Asn1326Thr
NM_001079817.1:c.3941A>C	NP_001073285.1:p.Asn1314Thr
NM_001079817.2:c.3941A>C	NP_001073285.1:p.Asn1314Thr
XM_011527988.1:c.4052A>C	XP_011526290.1:p.Asn1351Thr
XM_011527989.1:c.4016A>C	XP_011526291.1:p.Asn1339Thr
XM_011527988.2:c.3974A>C	XP_011526290.2:p.Asn1325Thr
XM_011527989.3:c.3938A>C	XP_011526291.2:p.Asn1313Thr
NM_000208.4:c.3977A>C MANE Select	NP_000199.2:p.Asn1326Thr
NM_001079817.3:c.3941A>C	NP_001073285.1:p.Asn1314Thr