Canonical Allele Identifier: CA403671244

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125422C>T (hg19) ; chr19:g.7125411C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125411C>T , CM000681.2:g.7125411C>T	GRCh38
NC_000019.9:g.7125422C>T , CM000681.1:g.7125422C>T	GRCh37
NC_000019.8:g.7076422C>T	NCBI36
NG_008852.2:g.173590G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3130G>A MANE Select	ENSP00000303830.4:p.Asp1044Asn
ENST00000302850.9:c.3130G>A	ENSP00000303830.4:p.Asp1044Asn
ENST00000341500.9:c.3094G>A	ENSP00000342838.4:p.Asp1032Asn
NM_000208.2:c.3130G>A	NP_000199.2:p.Asp1044Asn
NM_000208.3:c.3130G>A	NP_000199.2:p.Asp1044Asn
NM_001079817.1:c.3094G>A	NP_001073285.1:p.Asp1032Asn
NM_001079817.2:c.3094G>A	NP_001073285.1:p.Asp1032Asn
XM_011527988.1:c.3205G>A	XP_011526290.1:p.Asp1069Asn
XM_011527989.1:c.3169G>A	XP_011526291.1:p.Asp1057Asn
XM_011527988.2:c.3127G>A	XP_011526290.2:p.Asp1043Asn
XM_011527989.3:c.3091G>A	XP_011526291.2:p.Asp1031Asn
NM_000208.4:c.3130G>A MANE Select	NP_000199.2:p.Asp1044Asn
NM_001079817.3:c.3094G>A	NP_001073285.1:p.Asp1032Asn