Canonical Allele Identifier: CA403670839

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122946G>C (hg19) ; chr19:g.7122935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122935G>C , CM000681.2:g.7122935G>C	GRCh38
NC_000019.9:g.7122946G>C , CM000681.1:g.7122946G>C	GRCh37
NC_000019.8:g.7073946G>C	NCBI36
NG_008852.2:g.176066C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3313C>G MANE Select	ENSP00000303830.4:p.Leu1105Val
ENST00000302850.9:c.3313C>G	ENSP00000303830.4:p.Leu1105Val
ENST00000341500.9:c.3277C>G	ENSP00000342838.4:p.Leu1093Val
ENST00000593970.1:n.159C>G
ENST00000601099.1:n.224C>G
NM_000208.2:c.3313C>G	NP_000199.2:p.Leu1105Val
NM_000208.3:c.3313C>G	NP_000199.2:p.Leu1105Val
NM_001079817.1:c.3277C>G	NP_001073285.1:p.Leu1093Val
NM_001079817.2:c.3277C>G	NP_001073285.1:p.Leu1093Val
XM_011527988.1:c.3388C>G	XP_011526290.1:p.Leu1130Val
XM_011527989.1:c.3352C>G	XP_011526291.1:p.Leu1118Val
XM_011527988.2:c.3310C>G	XP_011526290.2:p.Leu1104Val
XM_011527989.3:c.3274C>G	XP_011526291.2:p.Leu1092Val
NM_000208.4:c.3313C>G MANE Select	NP_000199.2:p.Leu1105Val
NM_001079817.3:c.3277C>G	NP_001073285.1:p.Leu1093Val