Canonical Allele Identifier: CA359431020

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873709C>T (hg19) ; chr5:g.35873607C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873607C>T , CM000667.2:g.35873607C>T	GRCh38
NC_000005.9:g.35873709C>T , CM000667.1:g.35873709C>T	GRCh37
NC_000005.8:g.35909466C>T	NCBI36
NG_009567.1:g.21719C>T , LRG_74:g.21719C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.665C>T MANE Select	ENSP00000306157.3:p.Pro222Leu
ENST00000303115.7:c.665C>T	ENSP00000306157.3:p.Pro222Leu
ENST00000505093.1:c.74C>T	ENSP00000426069.1:p.Pro25Leu
ENST00000506850.5:c.665C>T	ENSP00000421207.1:p.Pro222Leu
ENST00000509668.1:n.407C>T
ENST00000514217.5:c.538-1905C>T	ENSP00000427688.1:n.538-1905C>T
NM_002185.3:c.665C>T	NP_002176.2:p.Pro222Leu
NR_120485.1:n.641-1905C>T
XM_005248299.2:c.665C>T	XP_005248356.1:p.Pro222Leu
XM_005248300.1:c.665C>T	XP_005248357.1:p.Pro222Leu
XM_011514037.1:c.665C>T	XP_011512339.1:p.Pro222Leu
NM_002185.4:c.665C>T	NP_002176.2:p.Pro222Leu
NR_120485.2:n.667-1905C>T
XM_005248299.4:c.665C>T	XP_005248356.1:p.Pro222Leu
NM_002185.5:c.665C>T MANE Select	NP_002176.2:p.Pro222Leu
NR_120485.3:n.625-1905C>T