Canonical Allele Identifier: CA993105736

Gene: INSR

Linked Data

• gnomAD v3: 19-7125520-TG-T
• gnomAD v4: 19-7125520-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125522del , CM000681.2:g.7125522del	GRCh38
NC_000019.9:g.7125533del , CM000681.1:g.7125533del	GRCh37
NC_000019.8:g.7076533del	NCBI36
NG_008852.2:g.173480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3020del MANE Select	ENSP00000303830.4:p.Pro1007HisfsTer?
ENST00000302850.9:c.3020del	ENSP00000303830.4:p.Pro1007HisfsTer?
ENST00000341500.9:c.2984del	ENSP00000342838.4:p.Pro995HisfsTer?
NM_000208.2:c.3020del	NP_000199.2:p.Pro1007HisfsTer?
NM_000208.3:c.3020del	NP_000199.2:p.Pro1007HisfsTer?
NM_001079817.1:c.2984del	NP_001073285.1:p.Pro995HisfsTer?
NM_001079817.2:c.2984del	NP_001073285.1:p.Pro995HisfsTer?
XM_011527988.1:c.3095del	XP_011526290.1:p.Pro1032HisfsTer?
XM_011527989.1:c.3059del	XP_011526291.1:p.Pro1020HisfsTer?
XM_011527988.2:c.3017del	XP_011526290.2:p.Pro1006HisfsTer?
XM_011527989.3:c.2981del	XP_011526291.2:p.Pro994HisfsTer?
NM_000208.4:c.3020del MANE Select	NP_000199.2:p.Pro1007HisfsTer?
NM_001079817.3:c.2984del	NP_001073285.1:p.Pro995HisfsTer?