Canonical Allele Identifier: CA403671059

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125335T>C (hg19) ; chr19:g.7125324T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125324T>C , CM000681.2:g.7125324T>C	GRCh38
NC_000019.9:g.7125335T>C , CM000681.1:g.7125335T>C	GRCh37
NC_000019.8:g.7076335T>C	NCBI36
NG_008852.2:g.173677A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3217A>G MANE Select	ENSP00000303830.4:p.Asn1073Asp
ENST00000302850.9:c.3217A>G	ENSP00000303830.4:p.Asn1073Asp
ENST00000341500.9:c.3181A>G	ENSP00000342838.4:p.Asn1061Asp
ENST00000593970.1:n.63A>G
NM_000208.2:c.3217A>G	NP_000199.2:p.Asn1073Asp
NM_000208.3:c.3217A>G	NP_000199.2:p.Asn1073Asp
NM_001079817.1:c.3181A>G	NP_001073285.1:p.Asn1061Asp
NM_001079817.2:c.3181A>G	NP_001073285.1:p.Asn1061Asp
XM_011527988.1:c.3292A>G	XP_011526290.1:p.Asn1098Asp
XM_011527989.1:c.3256A>G	XP_011526291.1:p.Asn1086Asp
XM_011527988.2:c.3214A>G	XP_011526290.2:p.Asn1072Asp
XM_011527989.3:c.3178A>G	XP_011526291.2:p.Asn1060Asp
NM_000208.4:c.3217A>G MANE Select	NP_000199.2:p.Asn1073Asp
NM_001079817.3:c.3181A>G	NP_001073285.1:p.Asn1061Asp