Canonical Allele Identifier: CA304843888

Gene: INSR

Linked Data

• dbSNP Id: rs755991906
• gnomAD v2: 19-7152653-T-TTG
• gnomAD v3: 19-7152642-T-TTG
• gnomAD v4: 19-7152642-T-TTG
• MyVariant Identifiers: chr19:g.7152653_7152654insTG (hg19) ; chr19:g.7152642_7152643insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152642_7152643insTG , CM000681.2:g.7152642_7152643insTG	GRCh38
NC_000019.9:g.7152653_7152654insTG , CM000681.1:g.7152653_7152654insTG	GRCh37
NC_000019.8:g.7103653_7103654insTG	NCBI36
NG_008852.2:g.146358_146359insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+83_2231+84insCA MANE Select	ENSP00000303830.4:n.2231+83_2231+84insCA
ENST00000302850.9:c.2231+83_2231+84insCA	ENSP00000303830.4:n.2231+83_2231+84insCA
ENST00000341500.9:c.2231+83_2231+84insCA	ENSP00000342838.4:n.2231+83_2231+84insCA
ENST00000598216.1:n.2289_2290insCA
NM_000208.2:c.2231+83_2231+84insCA	NP_000199.2:n.2231+83_2231+84insCA
NM_000208.3:c.2231+83_2231+84insCA	NP_000199.2:n.2231+83_2231+84insCA
NM_001079817.1:c.2231+83_2231+84insCA	NP_001073285.1:n.2231+83_2231+84insCA
NM_001079817.2:c.2231+83_2231+84insCA	NP_001073285.1:n.2231+83_2231+84insCA
XM_011527988.1:c.2309+83_2309+84insCA	XP_011526290.1:n.2309+83_2309+84insCA
XM_011527989.1:c.2309+83_2309+84insCA	XP_011526291.1:n.2309+83_2309+84insCA
XM_011527988.2:c.2231+83_2231+84insCA	XP_011526290.2:n.2231+83_2231+84insCA
XM_011527989.3:c.2231+83_2231+84insCA	XP_011526291.2:n.2231+83_2231+84insCA
NM_000208.4:c.2231+83_2231+84insCA MANE Select	NP_000199.2:n.2231+83_2231+84insCA
NM_001079817.3:c.2231+83_2231+84insCA	NP_001073285.1:n.2231+83_2231+84insCA