Canonical Allele Identifier: CA403671423

Gene: INSR

Linked Data

• dbSNP Id: rs1568430334
• MyVariant Identifiers: chr19:g.7125507C>G (hg19) ; chr19:g.7125496C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125496C>G , CM000681.2:g.7125496C>G	GRCh38
NC_000019.9:g.7125507C>G , CM000681.1:g.7125507C>G	GRCh37
NC_000019.8:g.7076507C>G	NCBI36
NG_008852.2:g.173505G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3045G>C MANE Select	ENSP00000303830.4:p.Glu1015Asp
ENST00000302850.9:c.3045G>C	ENSP00000303830.4:p.Glu1015Asp
ENST00000341500.9:c.3009G>C	ENSP00000342838.4:p.Glu1003Asp
NM_000208.2:c.3045G>C	NP_000199.2:p.Glu1015Asp
NM_000208.3:c.3045G>C	NP_000199.2:p.Glu1015Asp
NM_001079817.1:c.3009G>C	NP_001073285.1:p.Glu1003Asp
NM_001079817.2:c.3009G>C	NP_001073285.1:p.Glu1003Asp
XM_011527988.1:c.3120G>C	XP_011526290.1:p.Glu1040Asp
XM_011527989.1:c.3084G>C	XP_011526291.1:p.Glu1028Asp
XM_011527988.2:c.3042G>C	XP_011526290.2:p.Glu1014Asp
XM_011527989.3:c.3006G>C	XP_011526291.2:p.Glu1002Asp
NM_000208.4:c.3045G>C MANE Select	NP_000199.2:p.Glu1015Asp
NM_001079817.3:c.3009G>C	NP_001073285.1:p.Glu1003Asp