Canonical Allele Identifier: CA124220

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119563C>G , CM000681.2:g.7119563C>G	GRCh38
NC_000019.9:g.7119574C>G , CM000681.1:g.7119574C>G	GRCh37
NC_000019.8:g.7070574C>G	NCBI36
NG_008852.2:g.179438G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3680G>C MANE Select	ENSP00000303830.4:p.Trp1227Ser
ENST00000302850.9:c.3680G>C	ENSP00000303830.4:p.Trp1227Ser
ENST00000341500.9:c.3644G>C	ENSP00000342838.4:p.Trp1215Ser
NM_000208.2:c.3680G>C	NP_000199.2:p.Trp1227Ser
NM_000208.3:c.3680G>C	NP_000199.2:p.Trp1227Ser
NM_001079817.1:c.3644G>C	NP_001073285.1:p.Trp1215Ser
NM_001079817.2:c.3644G>C	NP_001073285.1:p.Trp1215Ser
XM_011527988.1:c.3755G>C	XP_011526290.1:p.Trp1252Ser
XM_011527989.1:c.3719G>C	XP_011526291.1:p.Trp1240Ser
XM_011527988.2:c.3677G>C	XP_011526290.2:p.Trp1226Ser
XM_011527989.3:c.3641G>C	XP_011526291.2:p.Trp1214Ser
NM_000208.4:c.3680G>C MANE Select	NP_000199.2:p.Trp1227Ser
NM_001079817.3:c.3644G>C	NP_001073285.1:p.Trp1215Ser