Canonical Allele Identifier: CA403671968

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132190G>A , CM000681.2:g.7132190G>A	GRCh38
NC_000019.9:g.7132201G>A , CM000681.1:g.7132201G>A	GRCh37
NC_000019.8:g.7083201G>A	NCBI36
NG_008852.2:g.166811C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.2810C>T MANE Select	NP_000199.2:p.Thr937Met
ENST00000302850.10:c.2810C>T MANE Select	ENSP00000303830.4:p.Thr937Met
NM_000208.2:c.2810C>T	NP_000199.2:p.Thr937Met
NM_000208.3:c.2810C>T	NP_000199.2:p.Thr937Met
NM_001079817.1:c.2774C>T	NP_001073285.1:p.Thr925Met
NM_001079817.2:c.2774C>T	NP_001073285.1:p.Thr925Met
NM_001079817.3:c.2774C>T	NP_001073285.1:p.Thr925Met
ENST00000302850.9:c.2810C>T	ENSP00000303830.4:p.Thr937Met
ENST00000341500.9:c.2774C>T	ENSP00000342838.4:p.Thr925Met
XM_011527988.1:c.2888C>T	XP_011526290.1:p.Thr963Met
XM_011527988.2:c.2810C>T	XP_011526290.2:p.Thr937Met
XM_011527989.1:c.2852C>T	XP_011526291.1:p.Thr951Met
XM_011527989.3:c.2774C>T	XP_011526291.2:p.Thr925Met