Canonical Allele Identifier: CA1139835401

Gene: CD247

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167439433C= , CM000663.2:g.167439433C=	GRCh38
NC_000001.10:g.167408670C= , CM000663.1:g.167408670C=	GRCh37
NC_000001.9:g.165675294C=	NCBI36
NG_007384.1:g.84177G= , LRG_36:g.84177G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392122.4:c.163-33G=	ENSP00000375969.3:n.163-33G=
ENST00000470379.2:c.-156G=	ENSP00000514807.1:n.-156G=
ENST00000476733.6:c.-156G=	ENSP00000514806.1:n.-156G=
ENST00000483825.6:n.227-33G=
ENST00000700105.1:c.163-33G=	ENSP00000514800.1:n.163-33G=
ENST00000700106.1:c.187-33G=	ENSP00000514802.1:n.187-33G=
ENST00000700107.1:c.187-33G=	ENSP00000514803.1:n.187-33G=
ENST00000700108.1:c.-123-33G=	ENSP00000514804.1:n.-123-33G=
ENST00000700109.1:c.-123-33G=	ENSP00000514805.1:n.-123-33G=
ENST00000700111.1:n.227-33G=
ENST00000700112.1:n.501-33G=
ENST00000700113.1:c.*444-33G=	ENSP00000514838.1:n.*444-33G=
ENST00000700134.1:c.163-33G=	ENSP00000514822.1:n.163-33G=
ENST00000700135.1:n.654-33G=
ENST00000700137.1:n.388-33G=
ENST00000700138.1:n.189-33G=
ENST00000700139.1:n.288-33G=
ENST00000700140.1:n.248-33G=
ENST00000700141.1:n.248-33G=
ENST00000700142.1:c.163-33G=	ENSP00000514823.1:n.163-33G=
ENST00000700143.1:n.127-33G=
ENST00000700155.1:c.-156G=	ENSP00000514827.1:n.-156G=
ENST00000700156.1:c.-123-33G=	ENSP00000514828.1:n.-123-33G=
ENST00000700157.1:c.7-33G=	ENSP00000514829.1:n.7-33G=
ENST00000700158.1:c.-123-33G=	ENSP00000514830.1:n.-123-33G=
ENST00000700159.1:c.163-33G=	ENSP00000514831.1:n.163-33G=
ENST00000700160.1:c.-123-33G=	ENSP00000514832.1:n.-123-33G=
ENST00000700161.1:c.-156G=	ENSP00000514833.1:n.-156G=
ENST00000700165.1:c.163-33G=	ENSP00000514836.1:n.163-33G=
ENST00000700166.1:n.159-33G=
ENST00000700167.1:c.163-33G=	ENSP00000514837.1:n.163-33G=
ENST00000362089.10:c.163-33G= MANE Select	ENSP00000354782.5:n.163-33G=
ENST00000362089.9:c.163-33G=	ENSP00000354782.5:n.163-33G=
ENST00000392122.3:c.163-33G=	ENSP00000375969.3:n.163-33G=
ENST00000470379.1:n.208G=
ENST00000476733.5:n.189G=
ENST00000483825.5:n.227-33G=
NM_000734.3:c.163-33G=	NP_000725.1:n.163-33G=
NM_198053.2:c.163-33G= , LRG_36t1:c.163-33G=	NP_932170.1:n.163-33G=
XM_011510144.1:c.187-33G=	XP_011508446.1:n.187-33G=
XM_011510145.1:c.187-33G=	XP_011508447.1:n.187-33G=
XM_011510144.2:c.187-33G=	XP_011508446.1:n.187-33G=
XM_017002800.1:c.256-33G=	XP_016858289.1:n.256-33G=
XM_017002801.1:c.256-33G=	XP_016858290.1:n.256-33G=
NM_000734.4:c.163-33G=	NP_000725.1:n.163-33G=
NM_001378515.1:c.256-33G=	NP_001365444.1:n.256-33G=
NM_001378516.1:c.256-33G=	NP_001365445.1:n.256-33G=
NM_198053.3:c.163-33G= MANE Select	NP_932170.1:n.163-33G=