Canonical Allele Identifier: CA403668310

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117124C>A (hg19) ; chr19:g.7117113C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117113C>A , CM000681.2:g.7117113C>A	GRCh38
NC_000019.9:g.7117124C>A , CM000681.1:g.7117124C>A	GRCh37
NC_000019.8:g.7068124C>A	NCBI36
NG_008852.2:g.181888G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4092G>T MANE Select	ENSP00000303830.4:p.Met1364Ile
ENST00000302850.9:c.4092G>T	ENSP00000303830.4:p.Met1364Ile
ENST00000341500.9:c.4056G>T	ENSP00000342838.4:p.Met1352Ile
NM_000208.2:c.4092G>T	NP_000199.2:p.Met1364Ile
NM_000208.3:c.4092G>T	NP_000199.2:p.Met1364Ile
NM_001079817.1:c.4056G>T	NP_001073285.1:p.Met1352Ile
NM_001079817.2:c.4056G>T	NP_001073285.1:p.Met1352Ile
XM_011527988.1:c.4167G>T	XP_011526290.1:p.Met1389Ile
XM_011527989.1:c.4131G>T	XP_011526291.1:p.Met1377Ile
XM_011527988.2:c.4089G>T	XP_011526290.2:p.Met1363Ile
XM_011527989.3:c.4053G>T	XP_011526291.2:p.Met1351Ile
NM_000208.4:c.4092G>T MANE Select	NP_000199.2:p.Met1364Ile
NM_001079817.3:c.4056G>T	NP_001073285.1:p.Met1352Ile