Canonical Allele Identifier: CA505216634

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120651G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120640G>A , CM000681.2:g.7120640G>A	GRCh38
NC_000019.9:g.7120651G>A , CM000681.1:g.7120651G>A	GRCh37
NC_000019.8:g.7071651G>A	NCBI36
NG_008852.2:g.178361C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3639C>T MANE Select	ENSP00000303830.4:p.Phe1213=
ENST00000302850.9:c.3639C>T	ENSP00000303830.4:p.Phe1213=
ENST00000341500.9:c.3603C>T	ENSP00000342838.4:p.Phe1201=
ENST00000601099.1:n.550C>T
NM_000208.2:c.3639C>T	NP_000199.2:p.Phe1213=
NM_000208.3:c.3639C>T	NP_000199.2:p.Phe1213=
NM_001079817.1:c.3603C>T	NP_001073285.1:p.Phe1201=
NM_001079817.2:c.3603C>T	NP_001073285.1:p.Phe1201=
XM_011527988.1:c.3714C>T	XP_011526290.1:p.Phe1238=
XM_011527989.1:c.3678C>T	XP_011526291.1:p.Phe1226=
XM_011527988.2:c.3636C>T	XP_011526290.2:p.Phe1212=
XM_011527989.3:c.3600C>T	XP_011526291.2:p.Phe1200=
NM_000208.4:c.3639C>T MANE Select	NP_000199.2:p.Phe1213=
NM_001079817.3:c.3603C>T	NP_001073285.1:p.Phe1201=