Canonical Allele Identifier: CA403671149

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125379G>T (hg19) ; chr19:g.7125368G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125368G>T , CM000681.2:g.7125368G>T	GRCh38
NC_000019.9:g.7125379G>T , CM000681.1:g.7125379G>T	GRCh37
NC_000019.8:g.7076379G>T	NCBI36
NG_008852.2:g.173633C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3173C>A MANE Select	ENSP00000303830.4:p.Thr1058Lys
ENST00000302850.9:c.3173C>A	ENSP00000303830.4:p.Thr1058Lys
ENST00000341500.9:c.3137C>A	ENSP00000342838.4:p.Thr1046Lys
ENST00000593970.1:n.19C>A
NM_000208.2:c.3173C>A	NP_000199.2:p.Thr1058Lys
NM_000208.3:c.3173C>A	NP_000199.2:p.Thr1058Lys
NM_001079817.1:c.3137C>A	NP_001073285.1:p.Thr1046Lys
NM_001079817.2:c.3137C>A	NP_001073285.1:p.Thr1046Lys
XM_011527988.1:c.3248C>A	XP_011526290.1:p.Thr1083Lys
XM_011527989.1:c.3212C>A	XP_011526291.1:p.Thr1071Lys
XM_011527988.2:c.3170C>A	XP_011526290.2:p.Thr1057Lys
XM_011527989.3:c.3134C>A	XP_011526291.2:p.Thr1045Lys
NM_000208.4:c.3173C>A MANE Select	NP_000199.2:p.Thr1058Lys
NM_001079817.3:c.3137C>A	NP_001073285.1:p.Thr1046Lys