Canonical Allele Identifier: CA2320790644

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172176_7172177delinsTG , CM000681.2:g.7172176_7172177delinsTG	GRCh38
NC_000019.9:g.7172187_7172188delinsTG , CM000681.1:g.7172187_7172188delinsTG	GRCh37
NC_000019.8:g.7123187_7123188delinsTG	NCBI36
NG_008852.2:g.126824_126825delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1268+113_1268+114delinsCA MANE Select	ENSP00000303830.4:n.1268+113_1268+114delinsCA
ENST00000302850.9:c.1268+113_1268+114delinsCA	ENSP00000303830.4:n.1268+113_1268+114delinsCA
ENST00000341500.9:c.1268+113_1268+114delinsCA	ENSP00000342838.4:n.1268+113_1268+114delinsCA
ENST00000598216.1:n.1243+113_1243+114delinsCA
NM_000208.2:c.1268+113_1268+114delinsCA	NP_000199.2:n.1268+113_1268+114delinsCA
NM_000208.3:c.1268+113_1268+114delinsCA	NP_000199.2:n.1268+113_1268+114delinsCA
NM_001079817.1:c.1268+113_1268+114delinsCA	NP_001073285.1:n.1268+113_1268+114delinsCA
NM_001079817.2:c.1268+113_1268+114delinsCA	NP_001073285.1:n.1268+113_1268+114delinsCA
XM_011527988.1:c.1346+113_1346+114delinsCA	XP_011526290.1:n.1346+113_1346+114delinsCA
XM_011527989.1:c.1346+113_1346+114delinsCA	XP_011526291.1:n.1346+113_1346+114delinsCA
XM_011527988.2:c.1268+113_1268+114delinsCA	XP_011526290.2:n.1268+113_1268+114delinsCA
XM_011527989.3:c.1268+113_1268+114delinsCA	XP_011526291.2:n.1268+113_1268+114delinsCA
NM_000208.4:c.1268+113_1268+114delinsCA MANE Select	NP_000199.2:n.1268+113_1268+114delinsCA
NM_001079817.3:c.1268+113_1268+114delinsCA	NP_001073285.1:n.1268+113_1268+114delinsCA