Canonical Allele Identifier: CA403672200

Gene: INSR

Linked Data

• COSMIC: COSM2728479 ; COSM2728480
• MyVariant Identifiers: chr19:g.7132315C>T (hg19) ; chr19:g.7132304C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132304C>T , CM000681.2:g.7132304C>T	GRCh38
NC_000019.9:g.7132315C>T , CM000681.1:g.7132315C>T	GRCh37
NC_000019.8:g.7083315C>T	NCBI36
NG_008852.2:g.166697G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2696G>A MANE Select	ENSP00000303830.4:p.Cys899Tyr
ENST00000302850.9:c.2696G>A	ENSP00000303830.4:p.Cys899Tyr
ENST00000341500.9:c.2660G>A	ENSP00000342838.4:p.Cys887Tyr
NM_000208.2:c.2696G>A	NP_000199.2:p.Cys899Tyr
NM_000208.3:c.2696G>A	NP_000199.2:p.Cys899Tyr
NM_001079817.1:c.2660G>A	NP_001073285.1:p.Cys887Tyr
NM_001079817.2:c.2660G>A	NP_001073285.1:p.Cys887Tyr
XM_011527988.1:c.2774G>A	XP_011526290.1:p.Cys925Tyr
XM_011527989.1:c.2738G>A	XP_011526291.1:p.Cys913Tyr
XM_011527988.2:c.2696G>A	XP_011526290.2:p.Cys899Tyr
XM_011527989.3:c.2660G>A	XP_011526291.2:p.Cys887Tyr
NM_000208.4:c.2696G>A MANE Select	NP_000199.2:p.Cys899Tyr
NM_001079817.3:c.2660G>A	NP_001073285.1:p.Cys887Tyr