Canonical Allele Identifier: CA403669466

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120701G>T (hg19) ; chr19:g.7120690G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120690G>T , CM000681.2:g.7120690G>T	GRCh38
NC_000019.9:g.7120701G>T , CM000681.1:g.7120701G>T	GRCh37
NC_000019.8:g.7071701G>T	NCBI36
NG_008852.2:g.178311C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3589C>A MANE Select	ENSP00000303830.4:p.Leu1197Met
ENST00000302850.9:c.3589C>A	ENSP00000303830.4:p.Leu1197Met
ENST00000341500.9:c.3553C>A	ENSP00000342838.4:p.Leu1185Met
ENST00000601099.1:n.500C>A
NM_000208.2:c.3589C>A	NP_000199.2:p.Leu1197Met
NM_000208.3:c.3589C>A	NP_000199.2:p.Leu1197Met
NM_001079817.1:c.3553C>A	NP_001073285.1:p.Leu1185Met
NM_001079817.2:c.3553C>A	NP_001073285.1:p.Leu1185Met
XM_011527988.1:c.3664C>A	XP_011526290.1:p.Leu1222Met
XM_011527989.1:c.3628C>A	XP_011526291.1:p.Leu1210Met
XM_011527988.2:c.3586C>A	XP_011526290.2:p.Leu1196Met
XM_011527989.3:c.3550C>A	XP_011526291.2:p.Leu1184Met
NM_000208.4:c.3589C>A MANE Select	NP_000199.2:p.Leu1197Met
NM_001079817.3:c.3553C>A	NP_001073285.1:p.Leu1185Met