Canonical Allele Identifier: CA2561221554

Gene: CD247

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167451106_167451107del , CM000663.2:g.167451106_167451107del	GRCh38
NC_000001.10:g.167420343_167420344del , CM000663.1:g.167420343_167420344del	GRCh37
NC_000001.9:g.165686967_165686968del	NCBI36
NG_007384.1:g.72504_72505del , LRG_36:g.72504_72505del

Transcript Alleles

HGVS	Amino-acid change
ENST00000392122.4:c.59-10339_59-10338del	ENSP00000375969.3:n.59-10339_59-10338del
ENST00000479979.2:n.132-10339_132-10338del
ENST00000483825.6:n.123-10339_123-10338del
ENST00000700105.1:c.59-10339_59-10338del	ENSP00000514800.1:n.59-10339_59-10338del
ENST00000700106.1:c.-63-2619_-63-2618del	ENSP00000514802.1:n.-63-2619_-63-2618del
ENST00000700107.1:c.-63-2619_-63-2618del	ENSP00000514803.1:n.-63-2619_-63-2618del
ENST00000700108.1:c.-536-6655_-536-6654del	ENSP00000514804.1:n.-536-6655_-536-6654de...
ENST00000700109.1:c.-536-6655_-536-6654del	ENSP00000514805.1:n.-536-6655_-536-6654de...
ENST00000700111.1:n.123-10339_123-10338del
ENST00000700113.1:c.*340-10339_*340-10338del	ENSP00000514838.1:n.*340-10339_*340-10338...
ENST00000700134.1:c.59-10339_59-10338del	ENSP00000514822.1:n.59-10339_59-10338del
ENST00000700138.1:n.84+5071_84+5072del
ENST00000700139.1:n.184-10339_184-10338del
ENST00000700140.1:n.144-10339_144-10338del
ENST00000700141.1:n.144-10339_144-10338del
ENST00000700142.1:c.59-10339_59-10338del	ENSP00000514823.1:n.59-10339_59-10338del
ENST00000700143.1:n.22+4374_22+4375del
ENST00000700158.1:c.-228+4374_-228+4375del	ENSP00000514830.1:n.-228+4374_-228+4375de...
ENST00000700159.1:c.59-10339_59-10338del	ENSP00000514831.1:n.59-10339_59-10338del
ENST00000700160.1:c.-227-10339_-227-10338del	ENSP00000514832.1:n.-227-10339_-227-10338...
ENST00000700165.1:c.59-10339_59-10338del	ENSP00000514836.1:n.59-10339_59-10338del
ENST00000700166.1:n.54+1980_54+1981del
ENST00000700167.1:c.59-10339_59-10338del	ENSP00000514837.1:n.59-10339_59-10338del
ENST00000700169.1:n.62+4374_62+4375del
ENST00000362089.10:c.59-10339_59-10338del MANE Select	ENSP00000354782.5:n.59-10339_59-10338del
ENST00000362089.9:c.59-10339_59-10338del	ENSP00000354782.5:n.59-10339_59-10338del
ENST00000392122.3:c.59-10339_59-10338del	ENSP00000375969.3:n.59-10339_59-10338del
ENST00000479979.1:n.204-10339_204-10338del
ENST00000483825.5:n.123-10339_123-10338del
NM_000734.3:c.59-10339_59-10338del	NP_000725.1:n.59-10339_59-10338del
NM_198053.2:c.59-10339_59-10338del , LRG_36t1:c.59-10339_59-10338del	NP_932170.1:n.59-10339_59-10338del
XM_011510144.1:c.-63-2619_-63-2618del	XP_011508446.1:n.-63-2619_-63-2618del
XM_011510145.1:c.-63-2619_-63-2618del	XP_011508447.1:n.-63-2619_-63-2618del
XM_011510144.2:c.-63-2619_-63-2618del	XP_011508446.1:n.-63-2619_-63-2618del
XM_017002800.1:c.152-10339_152-10338del	XP_016858289.1:n.152-10339_152-10338del
XM_017002801.1:c.152-10339_152-10338del	XP_016858290.1:n.152-10339_152-10338del
NM_000734.4:c.59-10339_59-10338del	NP_000725.1:n.59-10339_59-10338del
NM_001378515.1:c.152-10339_152-10338del	NP_001365444.1:n.152-10339_152-10338del
NM_001378516.1:c.152-10339_152-10338del	NP_001365445.1:n.152-10339_152-10338del
NM_198053.3:c.59-10339_59-10338del MANE Select	NP_932170.1:n.59-10339_59-10338del