Canonical Allele Identifier: CA1140886877

Gene: CD247

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167439355G= , CM000663.2:g.167439355G=	GRCh38
NC_000001.10:g.167408592G= , CM000663.1:g.167408592G=	GRCh37
NC_000001.9:g.165675216G=	NCBI36
NG_007384.1:g.84255C= , LRG_36:g.84255C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392122.4:c.208C=	ENSP00000375969.3:p.Gln70=
ENST00000470379.2:c.-78C=	ENSP00000514807.1:n.-78C=
ENST00000476733.6:c.-78C=	ENSP00000514806.1:n.-78C=
ENST00000483825.6:n.272C=
ENST00000700105.1:c.208C=	ENSP00000514800.1:p.Gln70=
ENST00000700106.1:c.232C=	ENSP00000514802.1:p.Gln78=
ENST00000700107.1:c.232C=	ENSP00000514803.1:p.Gln78=
ENST00000700108.1:c.-78C=	ENSP00000514804.1:n.-78C=
ENST00000700109.1:c.-78C=	ENSP00000514805.1:n.-78C=
ENST00000700111.1:n.272C=
ENST00000700112.1:n.546C=
ENST00000700113.1:c.*489C=	ENSP00000514838.1:n.*489C=
ENST00000700134.1:c.208C=	ENSP00000514822.1:p.Gln70=
ENST00000700135.1:n.699C=
ENST00000700137.1:n.433C=
ENST00000700138.1:n.234C=
ENST00000700139.1:n.333C=
ENST00000700140.1:n.293C=
ENST00000700141.1:n.293C=
ENST00000700142.1:c.208C=	ENSP00000514823.1:p.Gln70=
ENST00000700143.1:n.172C=
ENST00000700155.1:c.-78C=	ENSP00000514827.1:n.-78C=
ENST00000700156.1:c.-78C=	ENSP00000514828.1:n.-78C=
ENST00000700157.1:c.52C=	ENSP00000514829.1:p.Gln18=
ENST00000700158.1:c.-78C=	ENSP00000514830.1:n.-78C=
ENST00000700159.1:c.208C=	ENSP00000514831.1:p.Gln70=
ENST00000700160.1:c.-78C=	ENSP00000514832.1:n.-78C=
ENST00000700161.1:c.-78C=	ENSP00000514833.1:n.-78C=
ENST00000700165.1:c.208C=	ENSP00000514836.1:p.Gln70=
ENST00000700166.1:n.204C=
ENST00000700167.1:c.208C=	ENSP00000514837.1:p.Gln70=
ENST00000362089.10:c.208C= MANE Select	ENSP00000354782.5:p.Gln70=
ENST00000362089.9:c.208C=	ENSP00000354782.5:p.Gln70=
ENST00000392122.3:c.208C=	ENSP00000375969.3:p.Gln70=
ENST00000470379.1:n.286C=
ENST00000476733.5:n.267C=
ENST00000483825.5:n.272C=
NM_000734.3:c.208C=	NP_000725.1:p.Gln70=
NM_198053.2:c.208C= , LRG_36t1:c.208C=	NP_932170.1:p.Gln70=
XM_011510144.1:c.232C=	XP_011508446.1:p.Gln78=
XM_011510145.1:c.232C=	XP_011508447.1:p.Gln78=
XM_011510144.2:c.232C=	XP_011508446.1:p.Gln78=
XM_017002800.1:c.301C=	XP_016858289.1:p.Gln101=
XM_017002801.1:c.301C=	XP_016858290.1:p.Gln101=
NM_000734.4:c.208C=	NP_000725.1:p.Gln70=
NM_001378515.1:c.301C=	NP_001365444.1:p.Gln101=
NM_001378516.1:c.301C=	NP_001365445.1:p.Gln101=
NM_198053.3:c.208C= MANE Select	NP_932170.1:p.Gln70=