Canonical Allele Identifier: CA884178279

Gene: INSR

Linked Data

• dbSNP Id: rs1353689861
• gnomAD v4: 19-7128972-AAT-A
• MyVariant Identifiers: chr19:g.7128984_7128985del (hg19) ; chr19:g.7128973_7128974del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128977_7128978del , CM000681.2:g.7128977_7128978del	GRCh38
NC_000019.9:g.7128988_7128989del , CM000681.1:g.7128988_7128989del	GRCh37
NC_000019.8:g.7079988_7079989del	NCBI36
NG_008852.2:g.170027_170028del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2843-20_2843-19del MANE Select	ENSP00000303830.4:n.2843-20_2843-19del
ENST00000302850.9:c.2843-20_2843-19del	ENSP00000303830.4:n.2843-20_2843-19del
ENST00000341500.9:c.2807-20_2807-19del	ENSP00000342838.4:n.2807-20_2807-19del
NM_000208.2:c.2843-20_2843-19del	NP_000199.2:n.2843-20_2843-19del
NM_000208.3:c.2843-20_2843-19del	NP_000199.2:n.2843-20_2843-19del
NM_001079817.1:c.2807-20_2807-19del	NP_001073285.1:n.2807-20_2807-19del
NM_001079817.2:c.2807-20_2807-19del	NP_001073285.1:n.2807-20_2807-19del
XM_011527988.1:c.2921-23_2921-22del	XP_011526290.1:n.2921-23_2921-22del
XM_011527989.1:c.2885-23_2885-22del	XP_011526291.1:n.2885-23_2885-22del
XM_011527988.2:c.2843-23_2843-22del	XP_011526290.2:n.2843-23_2843-22del
XM_011527989.3:c.2807-23_2807-22del	XP_011526291.2:n.2807-23_2807-22del
NM_000208.4:c.2843-20_2843-19del MANE Select	NP_000199.2:n.2843-20_2843-19del
NM_001079817.3:c.2807-20_2807-19del	NP_001073285.1:n.2807-20_2807-19del