Canonical Allele Identifier: CA631723701

Gene: INSR

Linked Data

• dbSNP Id: rs1371102192
• gnomAD v2: 19-7152527-T-TAAAA
• gnomAD v3: 19-7152516-T-TAAAA
• gnomAD v4: 19-7152516-T-TAAAA
• MyVariant Identifiers: chr19:g.7152527_7152528insAAAA (hg19) ; chr19:g.7152516_7152517insAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152516_7152517insAAAA , CM000681.2:g.7152516_7152517insAAAA	GRCh38
NC_000019.9:g.7152527_7152528insAAAA , CM000681.1:g.7152527_7152528insAAAA	GRCh37
NC_000019.8:g.7103527_7103528insAAAA	NCBI36
NG_008852.2:g.146484_146485insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+209_2231+210insTTTT MANE Select	ENSP00000303830.4:n.2231+209_2231+210insTTTT
ENST00000302850.9:c.2231+209_2231+210insTTTT	ENSP00000303830.4:n.2231+209_2231+210insTTTT
ENST00000341500.9:c.2231+209_2231+210insTTTT	ENSP00000342838.4:n.2231+209_2231+210insTTTT
ENST00000598216.1:n.2415_2416insTTTT
NM_000208.2:c.2231+209_2231+210insTTTT	NP_000199.2:n.2231+209_2231+210insTTTT
NM_000208.3:c.2231+209_2231+210insTTTT	NP_000199.2:n.2231+209_2231+210insTTTT
NM_001079817.1:c.2231+209_2231+210insTTTT	NP_001073285.1:n.2231+209_2231+210insTTTT
NM_001079817.2:c.2231+209_2231+210insTTTT	NP_001073285.1:n.2231+209_2231+210insTTTT
XM_011527988.1:c.2309+209_2309+210insTTTT	XP_011526290.1:n.2309+209_2309+210insTTTT
XM_011527989.1:c.2309+209_2309+210insTTTT	XP_011526291.1:n.2309+209_2309+210insTTTT
XM_011527988.2:c.2231+209_2231+210insTTTT	XP_011526290.2:n.2231+209_2231+210insTTTT
XM_011527989.3:c.2231+209_2231+210insTTTT	XP_011526291.2:n.2231+209_2231+210insTTTT
NM_000208.4:c.2231+209_2231+210insTTTT MANE Select	NP_000199.2:n.2231+209_2231+210insTTTT
NM_001079817.3:c.2231+209_2231+210insTTTT	NP_001073285.1:n.2231+209_2231+210insTTTT