Canonical Allele Identifier: CA403671185

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125397G>T (hg19) ; chr19:g.7125386G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125386G>T , CM000681.2:g.7125386G>T	GRCh38
NC_000019.9:g.7125397G>T , CM000681.1:g.7125397G>T	GRCh37
NC_000019.8:g.7076397G>T	NCBI36
NG_008852.2:g.173615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3155C>A MANE Select	ENSP00000303830.4:p.Thr1052Asn
ENST00000302850.9:c.3155C>A	ENSP00000303830.4:p.Thr1052Asn
ENST00000341500.9:c.3119C>A	ENSP00000342838.4:p.Thr1040Asn
ENST00000593970.1:n.1C>A
NM_000208.2:c.3155C>A	NP_000199.2:p.Thr1052Asn
NM_000208.3:c.3155C>A	NP_000199.2:p.Thr1052Asn
NM_001079817.1:c.3119C>A	NP_001073285.1:p.Thr1040Asn
NM_001079817.2:c.3119C>A	NP_001073285.1:p.Thr1040Asn
XM_011527988.1:c.3230C>A	XP_011526290.1:p.Thr1077Asn
XM_011527989.1:c.3194C>A	XP_011526291.1:p.Thr1065Asn
XM_011527988.2:c.3152C>A	XP_011526290.2:p.Thr1051Asn
XM_011527989.3:c.3116C>A	XP_011526291.2:p.Thr1039Asn
NM_000208.4:c.3155C>A MANE Select	NP_000199.2:p.Thr1052Asn
NM_001079817.3:c.3119C>A	NP_001073285.1:p.Thr1040Asn