Canonical Allele Identifier: CA443891912

Gene: IL7R

Linked Data

• gnomAD v4: 5-35873515-G-A
• MyVariant Identifiers: chr5:g.35873617G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873515G>A , CM000667.2:g.35873515G>A	GRCh38
NC_000005.9:g.35873617G>A , CM000667.1:g.35873617G>A	GRCh37
NC_000005.8:g.35909374G>A	NCBI36
NG_009567.1:g.21627G>A , LRG_74:g.21627G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.573G>A MANE Select	ENSP00000306157.3:p.Leu191=
ENST00000303115.7:c.573G>A	ENSP00000306157.3:p.Leu191=
ENST00000506850.5:c.573G>A	ENSP00000421207.1:p.Leu191=
ENST00000509668.1:n.315G>A
ENST00000514217.5:c.538-1997G>A	ENSP00000427688.1:n.538-1997G>A
NM_002185.3:c.573G>A	NP_002176.2:p.Leu191=
NR_120485.1:n.641-1997G>A
XM_005248299.2:c.573G>A	XP_005248356.1:p.Leu191=
XM_005248300.1:c.573G>A	XP_005248357.1:p.Leu191=
XM_011514037.1:c.573G>A	XP_011512339.1:p.Leu191=
NM_002185.4:c.573G>A	NP_002176.2:p.Leu191=
NR_120485.2:n.667-1997G>A
XM_005248299.4:c.573G>A	XP_005248356.1:p.Leu191=
NM_002185.5:c.573G>A MANE Select	NP_002176.2:p.Leu191=
NR_120485.3:n.625-1997G>A