Canonical Allele Identifier: CA403669383

Gene: INSR

Linked Data

• gnomAD v4: 19-7120651-C-T
• MyVariant Identifiers: chr19:g.7120662C>T (hg19) ; chr19:g.7120651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120651C>T , CM000681.2:g.7120651C>T	GRCh38
NC_000019.9:g.7120662C>T , CM000681.1:g.7120662C>T	GRCh37
NC_000019.8:g.7071662C>T	NCBI36
NG_008852.2:g.178350G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3628G>A MANE Select	ENSP00000303830.4:p.Asp1210Asn
ENST00000302850.9:c.3628G>A	ENSP00000303830.4:p.Asp1210Asn
ENST00000341500.9:c.3592G>A	ENSP00000342838.4:p.Asp1198Asn
ENST00000601099.1:n.539G>A
NM_000208.2:c.3628G>A	NP_000199.2:p.Asp1210Asn
NM_000208.3:c.3628G>A	NP_000199.2:p.Asp1210Asn
NM_001079817.1:c.3592G>A	NP_001073285.1:p.Asp1198Asn
NM_001079817.2:c.3592G>A	NP_001073285.1:p.Asp1198Asn
XM_011527988.1:c.3703G>A	XP_011526290.1:p.Asp1235Asn
XM_011527989.1:c.3667G>A	XP_011526291.1:p.Asp1223Asn
XM_011527988.2:c.3625G>A	XP_011526290.2:p.Asp1209Asn
XM_011527989.3:c.3589G>A	XP_011526291.2:p.Asp1197Asn
NM_000208.4:c.3628G>A MANE Select	NP_000199.2:p.Asp1210Asn
NM_001079817.3:c.3592G>A	NP_001073285.1:p.Asp1198Asn