Canonical Allele Identifier: CA403671166

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125386C>T (hg19) ; chr19:g.7125375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125375C>T , CM000681.2:g.7125375C>T	GRCh38
NC_000019.9:g.7125386C>T , CM000681.1:g.7125386C>T	GRCh37
NC_000019.8:g.7076386C>T	NCBI36
NG_008852.2:g.173626G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3166G>A MANE Select	ENSP00000303830.4:p.Val1056Met
ENST00000302850.9:c.3166G>A	ENSP00000303830.4:p.Val1056Met
ENST00000341500.9:c.3130G>A	ENSP00000342838.4:p.Val1044Met
ENST00000593970.1:n.12G>A
NM_000208.2:c.3166G>A	NP_000199.2:p.Val1056Met
NM_000208.3:c.3166G>A	NP_000199.2:p.Val1056Met
NM_001079817.1:c.3130G>A	NP_001073285.1:p.Val1044Met
NM_001079817.2:c.3130G>A	NP_001073285.1:p.Val1044Met
XM_011527988.1:c.3241G>A	XP_011526290.1:p.Val1081Met
XM_011527989.1:c.3205G>A	XP_011526291.1:p.Val1069Met
XM_011527988.2:c.3163G>A	XP_011526290.2:p.Val1055Met
XM_011527989.3:c.3127G>A	XP_011526291.2:p.Val1043Met
NM_000208.4:c.3166G>A MANE Select	NP_000199.2:p.Val1056Met
NM_001079817.3:c.3130G>A	NP_001073285.1:p.Val1044Met