Canonical Allele Identifier: CA505217427

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128958G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128947G>T , CM000681.2:g.7128947G>T	GRCh38
NC_000019.9:g.7128958G>T , CM000681.1:g.7128958G>T	GRCh37
NC_000019.8:g.7079958G>T	NCBI36
NG_008852.2:g.170054C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2850C>A MANE Select	ENSP00000303830.4:p.Val950=
ENST00000302850.9:c.2850C>A	ENSP00000303830.4:p.Val950=
ENST00000341500.9:c.2814C>A	ENSP00000342838.4:p.Val938=
NM_000208.2:c.2850C>A	NP_000199.2:p.Val950=
NM_000208.3:c.2850C>A	NP_000199.2:p.Val950=
NM_001079817.1:c.2814C>A	NP_001073285.1:p.Val938=
NM_001079817.2:c.2814C>A	NP_001073285.1:p.Val938=
XM_011527988.1:c.2925C>A	XP_011526290.1:p.Val975=
XM_011527989.1:c.2889C>A	XP_011526291.1:p.Val963=
XM_011527988.2:c.2847C>A	XP_011526290.2:p.Val949=
XM_011527989.3:c.2811C>A	XP_011526291.2:p.Val937=
NM_000208.4:c.2850C>A MANE Select	NP_000199.2:p.Val950=
NM_001079817.3:c.2814C>A	NP_001073285.1:p.Val938=