Canonical Allele Identifier: CA403671256

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125428C>G (hg19) ; chr19:g.7125417C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125417C>G , CM000681.2:g.7125417C>G	GRCh38
NC_000019.9:g.7125428C>G , CM000681.1:g.7125428C>G	GRCh37
NC_000019.8:g.7076428C>G	NCBI36
NG_008852.2:g.173584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3124G>C MANE Select	ENSP00000303830.4:p.Ala1042Pro
ENST00000302850.9:c.3124G>C	ENSP00000303830.4:p.Ala1042Pro
ENST00000341500.9:c.3088G>C	ENSP00000342838.4:p.Ala1030Pro
NM_000208.2:c.3124G>C	NP_000199.2:p.Ala1042Pro
NM_000208.3:c.3124G>C	NP_000199.2:p.Ala1042Pro
NM_001079817.1:c.3088G>C	NP_001073285.1:p.Ala1030Pro
NM_001079817.2:c.3088G>C	NP_001073285.1:p.Ala1030Pro
XM_011527988.1:c.3199G>C	XP_011526290.1:p.Ala1067Pro
XM_011527989.1:c.3163G>C	XP_011526291.1:p.Ala1055Pro
XM_011527988.2:c.3121G>C	XP_011526290.2:p.Ala1041Pro
XM_011527989.3:c.3085G>C	XP_011526291.2:p.Ala1029Pro
NM_000208.4:c.3124G>C MANE Select	NP_000199.2:p.Ala1042Pro
NM_001079817.3:c.3088G>C	NP_001073285.1:p.Ala1030Pro