Canonical Allele Identifier: CA631680929

Gene: INSR

Linked Data

• gnomAD v2: 19-7212074-C-CCCAAGTCACAGACTCAGACTCTGGGGTGGATAA
• MyVariant Identifiers: chr19:g.7212074_7212075insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA (hg19) ; chr19:g.7212063_7212064insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212063_7212064insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA , CM000681.2:g.7212063_7212064insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA	GRCh38
NC_000019.9:g.7212074_7212075insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA , CM000681.1:g.7212074_7212075insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA	GRCh37
NC_000019.8:g.7163074_7163075insCCAAGTCACAGACTCAGACTCTGGGGTGGATAA	NCBI36
NG_008852.2:g.86937_86938insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG MANE Select	ENSP00000303830.4:n.653-27427_653-27426insTTATCCACCCCAGAGTCTG...
ENST00000302850.9:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	ENSP00000303830.4:n.653-27427_653-27426insTTATCCACCCCAGAGTCTG...
ENST00000341500.9:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	ENSP00000342838.4:n.653-27427_653-27426insTTATCCACCCCAGAGTCTG...
ENST00000598216.1:n.628-27427_628-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG
NM_000208.2:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	NP_000199.2:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTG...
NM_000208.3:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	NP_000199.2:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTG...
NM_001079817.1:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	NP_001073285.1:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGT...
NM_001079817.2:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	NP_001073285.1:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGT...
XM_011527988.1:c.731-27427_731-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	XP_011526290.1:n.731-27427_731-27426insTTATCCACCCCAGAGTCTGAGT...
XM_011527989.1:c.731-27427_731-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	XP_011526291.1:n.731-27427_731-27426insTTATCCACCCCAGAGTCTGAGT...
XM_011527988.2:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	XP_011526290.2:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGT...
XM_011527989.3:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	XP_011526291.2:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGT...
NM_000208.4:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG MANE Select	NP_000199.2:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTG...
NM_001079817.3:c.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGTCTGTGACTTGG	NP_001073285.1:n.653-27427_653-27426insTTATCCACCCCAGAGTCTGAGT...