Canonical Allele Identifier: CA631680907

Gene: INSR

Linked Data

• gnomAD v2: 19-7212070-C-CTGTTT
• gnomAD v3: 19-7212059-C-CTGTTT
• gnomAD v4: 19-7212059-C-CTGTTT
• MyVariant Identifiers: chr19:g.7212070_7212071insTGTTT (hg19) ; chr19:g.7212059_7212060insTGTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212059_7212060insTGTTT , CM000681.2:g.7212059_7212060insTGTTT	GRCh38
NC_000019.9:g.7212070_7212071insTGTTT , CM000681.1:g.7212070_7212071insTGTTT	GRCh37
NC_000019.8:g.7163070_7163071insTGTTT	NCBI36
NG_008852.2:g.86941_86942insAAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27423_653-27422insAAACA MANE Select	ENSP00000303830.4:n.653-27423_653-27422insAAACA
ENST00000302850.9:c.653-27423_653-27422insAAACA	ENSP00000303830.4:n.653-27423_653-27422insAAACA
ENST00000341500.9:c.653-27423_653-27422insAAACA	ENSP00000342838.4:n.653-27423_653-27422insAAACA
ENST00000598216.1:n.628-27423_628-27422insAAACA
NM_000208.2:c.653-27423_653-27422insAAACA	NP_000199.2:n.653-27423_653-27422insAAACA
NM_000208.3:c.653-27423_653-27422insAAACA	NP_000199.2:n.653-27423_653-27422insAAACA
NM_001079817.1:c.653-27423_653-27422insAAACA	NP_001073285.1:n.653-27423_653-27422insAAACA
NM_001079817.2:c.653-27423_653-27422insAAACA	NP_001073285.1:n.653-27423_653-27422insAAACA
XM_011527988.1:c.731-27423_731-27422insAAACA	XP_011526290.1:n.731-27423_731-27422insAAACA
XM_011527989.1:c.731-27423_731-27422insAAACA	XP_011526291.1:n.731-27423_731-27422insAAACA
XM_011527988.2:c.653-27423_653-27422insAAACA	XP_011526290.2:n.653-27423_653-27422insAAACA
XM_011527989.3:c.653-27423_653-27422insAAACA	XP_011526291.2:n.653-27423_653-27422insAAACA
NM_000208.4:c.653-27423_653-27422insAAACA MANE Select	NP_000199.2:n.653-27423_653-27422insAAACA
NM_001079817.3:c.653-27423_653-27422insAAACA	NP_001073285.1:n.653-27423_653-27422insAAACA