Canonical Allele Identifier: CA884186419

Gene: INSR

Linked Data

• dbSNP Id: rs1200831705
• MyVariant Identifiers: chr19:g.7150382_7150393del (hg19) ; chr19:g.7150371_7150382del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150371_7150382del , CM000681.2:g.7150371_7150382del	GRCh38
NC_000019.9:g.7150382_7150393del , CM000681.1:g.7150382_7150393del	GRCh37
NC_000019.8:g.7101382_7101393del	NCBI36
NG_008852.2:g.148619_148630del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+115_2267+126del MANE Select	ENSP00000303830.4:n.2267+115_2267+126del
ENST00000302850.9:c.2267+115_2267+126del	ENSP00000303830.4:n.2267+115_2267+126del
ENST00000341500.9:c.2231+2344_2231+2355del	ENSP00000342838.4:n.2231+2344_2231+2355del
NM_000208.2:c.2267+115_2267+126del	NP_000199.2:n.2267+115_2267+126del
NM_000208.3:c.2267+115_2267+126del	NP_000199.2:n.2267+115_2267+126del
NM_001079817.1:c.2231+2344_2231+2355del	NP_001073285.1:n.2231+2344_2231+2355del
NM_001079817.2:c.2231+2344_2231+2355del	NP_001073285.1:n.2231+2344_2231+2355del
XM_011527988.1:c.2345+115_2345+126del	XP_011526290.1:n.2345+115_2345+126del
XM_011527989.1:c.2309+2344_2309+2355del	XP_011526291.1:n.2309+2344_2309+2355del
XM_011527988.2:c.2267+115_2267+126del	XP_011526290.2:n.2267+115_2267+126del
XM_011527989.3:c.2231+2344_2231+2355del	XP_011526291.2:n.2231+2344_2231+2355del
NM_000208.4:c.2267+115_2267+126del MANE Select	NP_000199.2:n.2267+115_2267+126del
NM_001079817.3:c.2231+2344_2231+2355del	NP_001073285.1:n.2231+2344_2231+2355del