Canonical Allele Identifier: CA403671672

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128869C>A (hg19) ; chr19:g.7128858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128858C>A , CM000681.2:g.7128858C>A	GRCh38
NC_000019.9:g.7128869C>A , CM000681.1:g.7128869C>A	GRCh37
NC_000019.8:g.7079869C>A	NCBI36
NG_008852.2:g.170143G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2939G>T MANE Select	ENSP00000303830.4:p.Arg980Ile
ENST00000302850.9:c.2939G>T	ENSP00000303830.4:p.Arg980Ile
ENST00000341500.9:c.2903G>T	ENSP00000342838.4:p.Arg968Ile
NM_000208.2:c.2939G>T	NP_000199.2:p.Arg980Ile
NM_000208.3:c.2939G>T	NP_000199.2:p.Arg980Ile
NM_001079817.1:c.2903G>T	NP_001073285.1:p.Arg968Ile
NM_001079817.2:c.2903G>T	NP_001073285.1:p.Arg968Ile
XM_011527988.1:c.3014G>T	XP_011526290.1:p.Arg1005Ile
XM_011527989.1:c.2978G>T	XP_011526291.1:p.Arg993Ile
XM_011527988.2:c.2936G>T	XP_011526290.2:p.Arg979Ile
XM_011527989.3:c.2900G>T	XP_011526291.2:p.Arg967Ile
NM_000208.4:c.2939G>T MANE Select	NP_000199.2:p.Arg980Ile
NM_001079817.3:c.2903G>T	NP_001073285.1:p.Arg968Ile