Canonical Allele Identifier: CA403671022

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125319A>C (hg19) ; chr19:g.7125308A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125308A>C , CM000681.2:g.7125308A>C	GRCh38
NC_000019.9:g.7125319A>C , CM000681.1:g.7125319A>C	GRCh37
NC_000019.8:g.7076319A>C	NCBI36
NG_008852.2:g.173693T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3233T>G MANE Select	ENSP00000303830.4:p.Met1078Arg
ENST00000302850.9:c.3233T>G	ENSP00000303830.4:p.Met1078Arg
ENST00000341500.9:c.3197T>G	ENSP00000342838.4:p.Met1066Arg
ENST00000593970.1:n.79T>G
NM_000208.2:c.3233T>G	NP_000199.2:p.Met1078Arg
NM_000208.3:c.3233T>G	NP_000199.2:p.Met1078Arg
NM_001079817.1:c.3197T>G	NP_001073285.1:p.Met1066Arg
NM_001079817.2:c.3197T>G	NP_001073285.1:p.Met1066Arg
XM_011527988.1:c.3308T>G	XP_011526290.1:p.Met1103Arg
XM_011527989.1:c.3272T>G	XP_011526291.1:p.Met1091Arg
XM_011527988.2:c.3230T>G	XP_011526290.2:p.Met1077Arg
XM_011527989.3:c.3194T>G	XP_011526291.2:p.Met1065Arg
NM_000208.4:c.3233T>G MANE Select	NP_000199.2:p.Met1078Arg
NM_001079817.3:c.3197T>G	NP_001073285.1:p.Met1066Arg