Canonical Allele Identifier: CA1796223816

Gene: IL7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.78789641G= , CM000670.2:g.78789641G=	GRCh38
NC_000008.10:g.79701876G= , CM000670.1:g.79701876G=	GRCh37
NC_000008.9:g.79864431G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000880.4:c.147+8431C= MANE Select	NP_000871.1:n.147+8431C=
ENST00000263851.9:c.147+8431C= MANE Select	ENSP00000263851.4:n.147+8431C=
NM_000880.3:c.147+8431C=	NP_000871.1:n.147+8431C=
NM_001199886.1:c.147+8431C=	NP_001186815.1:n.147+8431C=
NM_001199886.2:c.147+8431C=	NP_001186815.1:n.147+8431C=
NM_001199887.1:c.147+8431C=	NP_001186816.1:n.147+8431C=
NM_001199887.2:c.147+8431C=	NP_001186816.1:n.147+8431C=
NM_001199888.1:c.147+8431C=	NP_001186817.1:n.147+8431C=
NM_001199888.2:c.147+8431C=	NP_001186817.1:n.147+8431C=
ENST00000263851.8:c.147+8431C=	ENSP00000263851.4:n.147+8431C=
ENST00000379113.6:c.147+8431C=	ENSP00000368408.3:n.147+8431C=
ENST00000518982.5:c.147+8431C=	ENSP00000430272.1:n.147+8431C=
ENST00000520215.5:c.91+8487C=	ENSP00000428364.1:n.91+8487C=
ENST00000520269.5:c.147+8431C=	ENSP00000427750.1:n.147+8431C=
ENST00000520317.1:c.91+8487C=	ENSP00000427800.1:n.91+8487C=
ENST00000541183.2:c.147+8431C=	ENSP00000438922.2:n.147+8431C=
ENST00000639719.1:c.147+8431C=	ENSP00000491060.1:n.147+8431C=
XM_011517521.1:c.147+8431C=	XP_011515823.1:n.147+8431C=
XM_011517522.1:c.147+8431C=	XP_011515824.1:n.147+8431C=
XM_011517522.3:c.147+8431C=	XP_011515824.1:n.147+8431C=
XM_011517523.1:c.147+8431C=	XP_011515825.1:n.147+8431C=
XM_011517523.3:c.147+8431C=	XP_011515825.1:n.147+8431C=
XM_017013397.2:c.-7+8487C=	XP_016868886.1:n.-7+8487C=