Canonical Allele Identifier: CA444093263

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867489G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867387G>T , CM000667.2:g.35867387G>T	GRCh38
NC_000005.9:g.35867489G>T , CM000667.1:g.35867489G>T	GRCh37
NC_000005.8:g.35903246G>T	NCBI36
NG_009567.1:g.15499G>T , LRG_74:g.15499G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.303G>T MANE Select	ENSP00000306157.3:p.Leu101=
ENST00000303115.7:c.303G>T	ENSP00000306157.3:p.Leu101=
ENST00000506850.5:c.303G>T	ENSP00000421207.1:p.Leu101=
ENST00000511031.1:n.437G>T
ENST00000511982.1:c.303G>T	ENSP00000425309.1:p.Leu101=
ENST00000514217.5:c.303G>T	ENSP00000427688.1:p.Leu101=
NM_002185.3:c.303G>T	NP_002176.2:p.Leu101=
NR_120485.1:n.406G>T
XM_005248299.2:c.303G>T	XP_005248356.1:p.Leu101=
XM_005248300.1:c.303G>T	XP_005248357.1:p.Leu101=
XM_011514037.1:c.303G>T	XP_011512339.1:p.Leu101=
NM_002185.4:c.303G>T	NP_002176.2:p.Leu101=
NR_120485.2:n.432G>T
XM_005248299.4:c.303G>T	XP_005248356.1:p.Leu101=
NM_002185.5:c.303G>T MANE Select	NP_002176.2:p.Leu101=
NR_120485.3:n.390G>T