Canonical Allele Identifier: CA2587920630

Gene: INSR

Linked Data

• gnomAD v4: 19-7116663-G-GTGTGGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116663_7116664insTGTGGGCA , CM000681.2:g.7116663_7116664insTGTGGGCA	GRCh38
NC_000019.9:g.7116674_7116675insTGTGGGCA , CM000681.1:g.7116674_7116675insTGTGGGCA	GRCh37
NC_000019.8:g.7067674_7067675insTGTGGGCA	NCBI36
NG_008852.2:g.182337_182338insTGCCCACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*392_*393insTGCCCACA MANE Select	ENSP00000303830.4:n.*392_*393insTGCCCACA
ENST00000302850.9:c.*392_*393insTGCCCACA	ENSP00000303830.4:n.*392_*393insTGCCCACA
ENST00000341500.9:c.*392_*393insTGCCCACA	ENSP00000342838.4:n.*392_*393insTGCCCACA
NM_000208.2:c.*392_*393insTGCCCACA	NP_000199.2:n.*392_*393insTGCCCACA
NM_000208.3:c.*392_*393insTGCCCACA	NP_000199.2:n.*392_*393insTGCCCACA
NM_001079817.1:c.*392_*393insTGCCCACA	NP_001073285.1:n.*392_*393insTGCCCACA
NM_001079817.2:c.*392_*393insTGCCCACA	NP_001073285.1:n.*392_*393insTGCCCACA
XM_011527988.1:c.*392_*393insTGCCCACA	XP_011526290.1:n.*392_*393insTGCCCACA
XM_011527989.1:c.*392_*393insTGCCCACA	XP_011526291.1:n.*392_*393insTGCCCACA
XM_011527988.2:c.*392_*393insTGCCCACA	XP_011526290.2:n.*392_*393insTGCCCACA
XM_011527989.3:c.*392_*393insTGCCCACA	XP_011526291.2:n.*392_*393insTGCCCACA
NM_000208.4:c.*392_*393insTGCCCACA MANE Select	NP_000199.2:n.*392_*393insTGCCCACA
NM_001079817.3:c.*392_*393insTGCCCACA	NP_001073285.1:n.*392_*393insTGCCCACA