Canonical Allele Identifier: CA403671470

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125529C>T (hg19) ; chr19:g.7125518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125518C>T , CM000681.2:g.7125518C>T	GRCh38
NC_000019.9:g.7125529C>T , CM000681.1:g.7125529C>T	GRCh37
NC_000019.8:g.7076529C>T	NCBI36
NG_008852.2:g.173483G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3023G>A MANE Select	ENSP00000303830.4:p.Cys1008Tyr
ENST00000302850.9:c.3023G>A	ENSP00000303830.4:p.Cys1008Tyr
ENST00000341500.9:c.2987G>A	ENSP00000342838.4:p.Cys996Tyr
NM_000208.2:c.3023G>A	NP_000199.2:p.Cys1008Tyr
NM_000208.3:c.3023G>A	NP_000199.2:p.Cys1008Tyr
NM_001079817.1:c.2987G>A	NP_001073285.1:p.Cys996Tyr
NM_001079817.2:c.2987G>A	NP_001073285.1:p.Cys996Tyr
XM_011527988.1:c.3098G>A	XP_011526290.1:p.Cys1033Tyr
XM_011527989.1:c.3062G>A	XP_011526291.1:p.Cys1021Tyr
XM_011527988.2:c.3020G>A	XP_011526290.2:p.Cys1007Tyr
XM_011527989.3:c.2984G>A	XP_011526291.2:p.Cys995Tyr
NM_000208.4:c.3023G>A MANE Select	NP_000199.2:p.Cys1008Tyr
NM_001079817.3:c.2987G>A	NP_001073285.1:p.Cys996Tyr