Canonical Allele Identifier: CA403670863

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122955C>G (hg19) ; chr19:g.7122944C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122944C>G , CM000681.2:g.7122944C>G	GRCh38
NC_000019.9:g.7122955C>G , CM000681.1:g.7122955C>G	GRCh37
NC_000019.8:g.7073955C>G	NCBI36
NG_008852.2:g.176057G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3304G>C MANE Select	ENSP00000303830.4:p.Val1102Leu
ENST00000302850.9:c.3304G>C	ENSP00000303830.4:p.Val1102Leu
ENST00000341500.9:c.3268G>C	ENSP00000342838.4:p.Val1090Leu
ENST00000593970.1:n.150G>C
ENST00000601099.1:n.215G>C
NM_000208.2:c.3304G>C	NP_000199.2:p.Val1102Leu
NM_000208.3:c.3304G>C	NP_000199.2:p.Val1102Leu
NM_001079817.1:c.3268G>C	NP_001073285.1:p.Val1090Leu
NM_001079817.2:c.3268G>C	NP_001073285.1:p.Val1090Leu
XM_011527988.1:c.3379G>C	XP_011526290.1:p.Val1127Leu
XM_011527989.1:c.3343G>C	XP_011526291.1:p.Val1115Leu
XM_011527988.2:c.3301G>C	XP_011526290.2:p.Val1101Leu
XM_011527989.3:c.3265G>C	XP_011526291.2:p.Val1089Leu
NM_000208.4:c.3304G>C MANE Select	NP_000199.2:p.Val1102Leu
NM_001079817.3:c.3268G>C	NP_001073285.1:p.Val1090Leu