Canonical Allele Identifier: CA505216675

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120690T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120679T>A , CM000681.2:g.7120679T>A	GRCh38
NC_000019.9:g.7120690T>A , CM000681.1:g.7120690T>A	GRCh37
NC_000019.8:g.7071690T>A	NCBI36
NG_008852.2:g.178322A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3600A>T MANE Select	ENSP00000303830.4:p.Val1200=
ENST00000302850.9:c.3600A>T	ENSP00000303830.4:p.Val1200=
ENST00000341500.9:c.3564A>T	ENSP00000342838.4:p.Val1188=
ENST00000601099.1:n.511A>T
NM_000208.2:c.3600A>T	NP_000199.2:p.Val1200=
NM_000208.3:c.3600A>T	NP_000199.2:p.Val1200=
NM_001079817.1:c.3564A>T	NP_001073285.1:p.Val1188=
NM_001079817.2:c.3564A>T	NP_001073285.1:p.Val1188=
XM_011527988.1:c.3675A>T	XP_011526290.1:p.Val1225=
XM_011527989.1:c.3639A>T	XP_011526291.1:p.Val1213=
XM_011527988.2:c.3597A>T	XP_011526290.2:p.Val1199=
XM_011527989.3:c.3561A>T	XP_011526291.2:p.Val1187=
NM_000208.4:c.3600A>T MANE Select	NP_000199.2:p.Val1200=
NM_001079817.3:c.3564A>T	NP_001073285.1:p.Val1188=