Canonical Allele Identifier: CA403671083

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125345A>C (hg19) ; chr19:g.7125334A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125334A>C , CM000681.2:g.7125334A>C	GRCh38
NC_000019.9:g.7125345A>C , CM000681.1:g.7125345A>C	GRCh37
NC_000019.8:g.7076345A>C	NCBI36
NG_008852.2:g.173667T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3207T>G MANE Select	ENSP00000303830.4:p.Ile1069Met
ENST00000302850.9:c.3207T>G	ENSP00000303830.4:p.Ile1069Met
ENST00000341500.9:c.3171T>G	ENSP00000342838.4:p.Ile1057Met
ENST00000593970.1:n.53T>G
NM_000208.2:c.3207T>G	NP_000199.2:p.Ile1069Met
NM_000208.3:c.3207T>G	NP_000199.2:p.Ile1069Met
NM_001079817.1:c.3171T>G	NP_001073285.1:p.Ile1057Met
NM_001079817.2:c.3171T>G	NP_001073285.1:p.Ile1057Met
XM_011527988.1:c.3282T>G	XP_011526290.1:p.Ile1094Met
XM_011527989.1:c.3246T>G	XP_011526291.1:p.Ile1082Met
XM_011527988.2:c.3204T>G	XP_011526290.2:p.Ile1068Met
XM_011527989.3:c.3168T>G	XP_011526291.2:p.Ile1056Met
NM_000208.4:c.3207T>G MANE Select	NP_000199.2:p.Ile1069Met
NM_001079817.3:c.3171T>G	NP_001073285.1:p.Ile1057Met