Canonical Allele Identifier: CA403671328

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125460T>G (hg19) ; chr19:g.7125449T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125449T>G , CM000681.2:g.7125449T>G	GRCh38
NC_000019.9:g.7125460T>G , CM000681.1:g.7125460T>G	GRCh37
NC_000019.8:g.7076460T>G	NCBI36
NG_008852.2:g.173552A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3092A>C MANE Select	ENSP00000303830.4:p.Gln1031Pro
ENST00000302850.9:c.3092A>C	ENSP00000303830.4:p.Gln1031Pro
ENST00000341500.9:c.3056A>C	ENSP00000342838.4:p.Gln1019Pro
NM_000208.2:c.3092A>C	NP_000199.2:p.Gln1031Pro
NM_000208.3:c.3092A>C	NP_000199.2:p.Gln1031Pro
NM_001079817.1:c.3056A>C	NP_001073285.1:p.Gln1019Pro
NM_001079817.2:c.3056A>C	NP_001073285.1:p.Gln1019Pro
XM_011527988.1:c.3167A>C	XP_011526290.1:p.Gln1056Pro
XM_011527989.1:c.3131A>C	XP_011526291.1:p.Gln1044Pro
XM_011527988.2:c.3089A>C	XP_011526290.2:p.Gln1030Pro
XM_011527989.3:c.3053A>C	XP_011526291.2:p.Gln1018Pro
NM_000208.4:c.3092A>C MANE Select	NP_000199.2:p.Gln1031Pro
NM_001079817.3:c.3056A>C	NP_001073285.1:p.Gln1019Pro