Canonical Allele Identifier: CA884186718

Gene: INSR

Linked Data

• dbSNP Id: rs1181741997
• MyVariant Identifiers: chr19:g.7152607_7152608insCTCC (hg19) ; chr19:g.7152596_7152597insCTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152597_7152600dup , CM000681.2:g.7152597_7152600dup	GRCh38
NC_000019.9:g.7152608_7152611dup , CM000681.1:g.7152608_7152611dup	GRCh37
NC_000019.8:g.7103608_7103611dup	NCBI36
NG_008852.2:g.146401_146404dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+126_2231+129dup MANE Select	ENSP00000303830.4:n.2231+126_2231+129dup
ENST00000302850.9:c.2231+126_2231+129dup	ENSP00000303830.4:n.2231+126_2231+129dup
ENST00000341500.9:c.2231+126_2231+129dup	ENSP00000342838.4:n.2231+126_2231+129dup
ENST00000598216.1:n.2332_2335dup
NM_000208.2:c.2231+126_2231+129dup	NP_000199.2:n.2231+126_2231+129dup
NM_000208.3:c.2231+126_2231+129dup	NP_000199.2:n.2231+126_2231+129dup
NM_001079817.1:c.2231+126_2231+129dup	NP_001073285.1:n.2231+126_2231+129dup
NM_001079817.2:c.2231+126_2231+129dup	NP_001073285.1:n.2231+126_2231+129dup
XM_011527988.1:c.2309+126_2309+129dup	XP_011526290.1:n.2309+126_2309+129dup
XM_011527989.1:c.2309+126_2309+129dup	XP_011526291.1:n.2309+126_2309+129dup
XM_011527988.2:c.2231+126_2231+129dup	XP_011526290.2:n.2231+126_2231+129dup
XM_011527989.3:c.2231+126_2231+129dup	XP_011526291.2:n.2231+126_2231+129dup
NM_000208.4:c.2231+126_2231+129dup MANE Select	NP_000199.2:n.2231+126_2231+129dup
NM_001079817.3:c.2231+126_2231+129dup	NP_001073285.1:n.2231+126_2231+129dup