Canonical Allele Identifier: CA505400295

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125522C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125511C>A , CM000681.2:g.7125511C>A	GRCh38
NC_000019.9:g.7125522C>A , CM000681.1:g.7125522C>A	GRCh37
NC_000019.8:g.7076522C>A	NCBI36
NG_008852.2:g.173490G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3030G>T MANE Select	ENSP00000303830.4:p.Val1010=
ENST00000302850.9:c.3030G>T	ENSP00000303830.4:p.Val1010=
ENST00000341500.9:c.2994G>T	ENSP00000342838.4:p.Val998=
NM_000208.2:c.3030G>T	NP_000199.2:p.Val1010=
NM_000208.3:c.3030G>T	NP_000199.2:p.Val1010=
NM_001079817.1:c.2994G>T	NP_001073285.1:p.Val998=
NM_001079817.2:c.2994G>T	NP_001073285.1:p.Val998=
XM_011527988.1:c.3105G>T	XP_011526290.1:p.Val1035=
XM_011527989.1:c.3069G>T	XP_011526291.1:p.Val1023=
XM_011527988.2:c.3027G>T	XP_011526290.2:p.Val1009=
XM_011527989.3:c.2991G>T	XP_011526291.2:p.Val997=
NM_000208.4:c.3030G>T MANE Select	NP_000199.2:p.Val1010=
NM_001079817.3:c.2994G>T	NP_001073285.1:p.Val998=