Canonical Allele Identifier: CA2695228019

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125420del , CM000681.2:g.7125420del	GRCh38
NC_000019.9:g.7125431del , CM000681.1:g.7125431del	GRCh37
NC_000019.8:g.7076431del	NCBI36
NG_008852.2:g.173582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3122del MANE Select	ENSP00000303830.4:p.Asn1041MetfsTer16
ENST00000302850.9:c.3122del	ENSP00000303830.4:p.Asn1041MetfsTer16
ENST00000341500.9:c.3086del	ENSP00000342838.4:p.Asn1029MetfsTer16
NM_000208.2:c.3122del	NP_000199.2:p.Asn1041MetfsTer16
NM_000208.3:c.3122del	NP_000199.2:p.Asn1041MetfsTer16
NM_001079817.1:c.3086del	NP_001073285.1:p.Asn1029MetfsTer16
NM_001079817.2:c.3086del	NP_001073285.1:p.Asn1029MetfsTer16
XM_011527988.1:c.3197del	XP_011526290.1:p.Asn1066MetfsTer16
XM_011527989.1:c.3161del	XP_011526291.1:p.Asn1054MetfsTer16
XM_011527988.2:c.3119del	XP_011526290.2:p.Asn1040MetfsTer16
XM_011527989.3:c.3083del	XP_011526291.2:p.Asn1028MetfsTer16
NM_000208.4:c.3122del MANE Select	NP_000199.2:p.Asn1041MetfsTer16
NM_001079817.3:c.3086del	NP_001073285.1:p.Asn1029MetfsTer16