Canonical Allele Identifier: CA403671442

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125515G>T (hg19) ; chr19:g.7125504G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125504G>T , CM000681.2:g.7125504G>T	GRCh38
NC_000019.9:g.7125515G>T , CM000681.1:g.7125515G>T	GRCh37
NC_000019.8:g.7076515G>T	NCBI36
NG_008852.2:g.173497C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3037C>A MANE Select	ENSP00000303830.4:p.Pro1013Thr
ENST00000302850.9:c.3037C>A	ENSP00000303830.4:p.Pro1013Thr
ENST00000341500.9:c.3001C>A	ENSP00000342838.4:p.Pro1001Thr
NM_000208.2:c.3037C>A	NP_000199.2:p.Pro1013Thr
NM_000208.3:c.3037C>A	NP_000199.2:p.Pro1013Thr
NM_001079817.1:c.3001C>A	NP_001073285.1:p.Pro1001Thr
NM_001079817.2:c.3001C>A	NP_001073285.1:p.Pro1001Thr
XM_011527988.1:c.3112C>A	XP_011526290.1:p.Pro1038Thr
XM_011527989.1:c.3076C>A	XP_011526291.1:p.Pro1026Thr
XM_011527988.2:c.3034C>A	XP_011526290.2:p.Pro1012Thr
XM_011527989.3:c.2998C>A	XP_011526291.2:p.Pro1000Thr
NM_000208.4:c.3037C>A MANE Select	NP_000199.2:p.Pro1013Thr
NM_001079817.3:c.3001C>A	NP_001073285.1:p.Pro1001Thr