Canonical Allele Identifier: CA403670822

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122939G>T (hg19) ; chr19:g.7122928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122928G>T , CM000681.2:g.7122928G>T	GRCh38
NC_000019.9:g.7122939G>T , CM000681.1:g.7122939G>T	GRCh37
NC_000019.8:g.7073939G>T	NCBI36
NG_008852.2:g.176073C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3320C>A MANE Select	ENSP00000303830.4:p.Ala1107Asp
ENST00000302850.9:c.3320C>A	ENSP00000303830.4:p.Ala1107Asp
ENST00000341500.9:c.3284C>A	ENSP00000342838.4:p.Ala1095Asp
ENST00000593970.1:n.166C>A
ENST00000601099.1:n.231C>A
NM_000208.2:c.3320C>A	NP_000199.2:p.Ala1107Asp
NM_000208.3:c.3320C>A	NP_000199.2:p.Ala1107Asp
NM_001079817.1:c.3284C>A	NP_001073285.1:p.Ala1095Asp
NM_001079817.2:c.3284C>A	NP_001073285.1:p.Ala1095Asp
XM_011527988.1:c.3395C>A	XP_011526290.1:p.Ala1132Asp
XM_011527989.1:c.3359C>A	XP_011526291.1:p.Ala1120Asp
XM_011527988.2:c.3317C>A	XP_011526290.2:p.Ala1106Asp
XM_011527989.3:c.3281C>A	XP_011526291.2:p.Ala1094Asp
NM_000208.4:c.3320C>A MANE Select	NP_000199.2:p.Ala1107Asp
NM_001079817.3:c.3284C>A	NP_001073285.1:p.Ala1095Asp