Canonical Allele Identifier: CA403670838

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122945A>C (hg19) ; chr19:g.7122934A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122934A>C , CM000681.2:g.7122934A>C	GRCh38
NC_000019.9:g.7122945A>C , CM000681.1:g.7122945A>C	GRCh37
NC_000019.8:g.7073945A>C	NCBI36
NG_008852.2:g.176067T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3314T>G MANE Select	ENSP00000303830.4:p.Leu1105Arg
ENST00000302850.9:c.3314T>G	ENSP00000303830.4:p.Leu1105Arg
ENST00000341500.9:c.3278T>G	ENSP00000342838.4:p.Leu1093Arg
ENST00000593970.1:n.160T>G
ENST00000601099.1:n.225T>G
NM_000208.2:c.3314T>G	NP_000199.2:p.Leu1105Arg
NM_000208.3:c.3314T>G	NP_000199.2:p.Leu1105Arg
NM_001079817.1:c.3278T>G	NP_001073285.1:p.Leu1093Arg
NM_001079817.2:c.3278T>G	NP_001073285.1:p.Leu1093Arg
XM_011527988.1:c.3389T>G	XP_011526290.1:p.Leu1130Arg
XM_011527989.1:c.3353T>G	XP_011526291.1:p.Leu1118Arg
XM_011527988.2:c.3311T>G	XP_011526290.2:p.Leu1104Arg
XM_011527989.3:c.3275T>G	XP_011526291.2:p.Leu1092Arg
NM_000208.4:c.3314T>G MANE Select	NP_000199.2:p.Leu1105Arg
NM_001079817.3:c.3278T>G	NP_001073285.1:p.Leu1093Arg