Canonical Allele Identifier: CA2531593428

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867470_35867471insTTTC , CM000667.2:g.35867470_35867471insTTTC	GRCh38
NC_000005.9:g.35867572_35867573insTTTC , CM000667.1:g.35867572_35867573insTTTC	GRCh37
NC_000005.8:g.35903329_35903330insTTTC	NCBI36
NG_009567.1:g.15582_15583insTTTC , LRG_74:g.15582_15583insTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+7_379+8insTTTC MANE Select	ENSP00000306157.3:n.379+7_379+8insTTTC
ENST00000303115.7:c.379+7_379+8insTTTC	ENSP00000306157.3:n.379+7_379+8insTTTC
ENST00000506850.5:c.379+7_379+8insTTTC	ENSP00000421207.1:n.379+7_379+8insTTTC
ENST00000511982.1:c.386_387insTTTC	ENSP00000425309.1:p.Lys129AsnfsTer26
ENST00000514217.5:c.379+7_379+8insTTTC	ENSP00000427688.1:n.379+7_379+8insTTTC
NM_002185.3:c.379+7_379+8insTTTC	NP_002176.2:n.379+7_379+8insTTTC
NR_120485.1:n.482+7_482+8insTTTC
XM_005248299.2:c.379+7_379+8insTTTC	XP_005248356.1:n.379+7_379+8insTTTC
XM_005248300.1:c.379+7_379+8insTTTC	XP_005248357.1:n.379+7_379+8insTTTC
XM_011514037.1:c.379+7_379+8insTTTC	XP_011512339.1:n.379+7_379+8insTTTC
NM_002185.4:c.379+7_379+8insTTTC	NP_002176.2:n.379+7_379+8insTTTC
NR_120485.2:n.508+7_508+8insTTTC
XM_005248299.4:c.379+7_379+8insTTTC	XP_005248356.1:n.379+7_379+8insTTTC
NM_002185.5:c.379+7_379+8insTTTC MANE Select	NP_002176.2:n.379+7_379+8insTTTC
NR_120485.3:n.466+7_466+8insTTTC