Canonical Allele Identifier: CA279689034

Gene: IL4R

Linked Data

• dbSNP Id: rs561552413
• gnomAD v2: 16-27376079-TAA-T
• gnomAD v3: 16-27364758-TAA-T
• gnomAD v4: 16-27364758-TAA-T
• MyVariant Identifiers: chr16:g.27376080_27376081del (hg19) ; chr16:g.27364759_27364760del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27364760_27364761del , CM000678.2:g.27364760_27364761del	GRCh38
NC_000016.9:g.27376081_27376082del , CM000678.1:g.27376081_27376082del	GRCh37
NC_000016.8:g.27283582_27283583del	NCBI36
NG_012086.1:g.55831_55832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.*930_*931del MANE Select	ENSP00000379111.2:n.*930_*931del
ENST00000170630.6:c.3363_3364del	ENSP00000170630.3:n.3363_3364del
ENST00000395762.6:c.*930_*931del	ENSP00000379111.2:n.*930_*931del
ENST00000543915.6:c.*930_*931del	ENSP00000441667.2:n.*930_*931del
NM_000418.3:c.*930_*931del	NP_000409.1:n.*930_*931del
NM_001257406.1:c.*930_*931del	NP_001244335.1:n.*930_*931del
NM_001257407.1:c.*930_*931del	NP_001244336.1:n.*930_*931del
NM_001257997.1:c.*930_*931del	NP_001244926.1:n.*930_*931del
XM_005255308.2:c.*930_*931del	XP_005255365.1:n.*930_*931del
XM_006721043.1:c.*930_*931del	XP_006721106.1:n.*930_*931del
XM_011545825.1:c.*930_*931del	XP_011544127.1:n.*930_*931del
XM_011545826.1:c.*930_*931del	XP_011544128.1:n.*930_*931del
XM_011545827.1:c.*930_*931del	XP_011544129.1:n.*930_*931del
XM_011545828.1:c.*930_*931del	XP_011544130.1:n.*930_*931del
XM_011545829.1:c.*930_*931del	XP_011544131.1:n.*930_*931del
XM_011545830.1:c.*930_*931del	XP_011544132.1:n.*930_*931del
XM_011545831.1:c.*930_*931del	XP_011544133.1:n.*930_*931del
XM_011545832.1:c.*930_*931del	XP_011544134.1:n.*930_*931del
XM_011545833.1:c.*930_*931del	XP_011544135.1:n.*930_*931del
XM_011545834.1:c.*930_*931del	XP_011544136.1:n.*930_*931del
XM_011545826.2:c.*930_*931del	XP_011544128.1:n.*930_*931del
XM_011545827.2:c.*930_*931del	XP_011544129.1:n.*930_*931del
XM_011545828.2:c.*930_*931del	XP_011544130.1:n.*930_*931del
XM_011545830.2:c.*930_*931del	XP_011544132.1:n.*930_*931del
XM_011545833.2:c.*930_*931del	XP_011544135.1:n.*930_*931del
XM_011545834.2:c.*930_*931del	XP_011544136.1:n.*930_*931del
NM_000418.4:c.*930_*931del MANE Select	NP_000409.1:n.*930_*931del
NM_001257406.2:c.*930_*931del	NP_001244335.1:n.*930_*931del
NM_001257407.2:c.*930_*931del	NP_001244336.1:n.*930_*931del
NM_001257997.2:c.*930_*931del	NP_001244926.1:n.*930_*931del