Canonical Allele Identifier: CA403670969

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125296C>G (hg19) ; chr19:g.7125285C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125285C>G , CM000681.2:g.7125285C>G	GRCh38
NC_000019.9:g.7125296C>G , CM000681.1:g.7125296C>G	GRCh37
NC_000019.8:g.7076296C>G	NCBI36
NG_008852.2:g.173716G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3256G>C MANE Select	ENSP00000303830.4:p.Val1086Leu
ENST00000302850.9:c.3256G>C	ENSP00000303830.4:p.Val1086Leu
ENST00000341500.9:c.3220G>C	ENSP00000342838.4:p.Val1074Leu
ENST00000593970.1:n.102G>C
NM_000208.2:c.3256G>C	NP_000199.2:p.Val1086Leu
NM_000208.3:c.3256G>C	NP_000199.2:p.Val1086Leu
NM_001079817.1:c.3220G>C	NP_001073285.1:p.Val1074Leu
NM_001079817.2:c.3220G>C	NP_001073285.1:p.Val1074Leu
XM_011527988.1:c.3331G>C	XP_011526290.1:p.Val1111Leu
XM_011527989.1:c.3295G>C	XP_011526291.1:p.Val1099Leu
XM_011527988.2:c.3253G>C	XP_011526290.2:p.Val1085Leu
XM_011527989.3:c.3217G>C	XP_011526291.2:p.Val1073Leu
NM_000208.4:c.3256G>C MANE Select	NP_000199.2:p.Val1086Leu
NM_001079817.3:c.3220G>C	NP_001073285.1:p.Val1074Leu